Schema for dbVar - Structural Variations in dbVar
  Database: dm6    Primary Table: dbvar_nstd134_call
VCF File: /gbdb/dm6/bbi/vcf/nstd134.submitted.variant_call.vcf.gz
Format description: The fields of a Variant Call Format data line
See the Variant Call Format specification for more details
fielddescription
chromAn identifier from the reference genome
posThe reference position, with the 1st base having position 1
idSemi-colon separated list of unique identifiers where available
refReference base(s)
altComma separated list of alternate non-reference alleles called on at least one of the samples
qualPhred-scaled quality score for the assertion made in ALT. i.e. give -10log_10 prob(call in ALT is wrong)
filterPASS if this position has passed all filters. Otherwise, a semicolon-separated list of codes for filters that fail
infoAdditional information encoded as a semicolon-separated series of short keys with optional comma-separated values
formatIf genotype columns are specified in header, a semicolon-separated list of of short keys starting with GT
genotypesIf genotype columns are specified in header, a tab-separated set of genotype column values; each value is a colon-separated list of values corresponding to keys in the format column

Sample Rows
 
chromposidrefaltqualfilterinfo
chr2L86452nssv13657626A..DBVARID;CALLID=chr2L_hc_tsxwm_alt_1;SVTYPE=INS;EXPERIMENT=1;SAMPLESET=1;END=86452;REGION=nsv2781011;AC=8;AF=0.018;AN=444
chr2L130271nssv13657262C..DBVARID;CALLID=chr2L_CNV_chr2L_130271_134470_alt_1;SVTYPE=DUP;EXPERIMENT=1;SAMPLESET=1;END=134469;REGION=nsv2780755;AC=90;AF=0.2 ...
chr2L263377nssv13657438G..DBVARID;CALLID=chr2L_hc_injed_alt_1;SVTYPE=DEL;EXPERIMENT=1;SAMPLESET=1;END=263445;REGION=nsv2781235;AC=170;AF=0.383;AN=444
chr2L285506nssv13657675G..DBVARID;CALLID=chr2L_hc_woiyg_alt_1;SVTYPE=INS;EXPERIMENT=1;SAMPLESET=1;END=285506;REGION=nsv2781297;AC=1;AF=0.002252;AN=444
chr2L429368nssv13657282C..DBVARID;CALLID=chr2L_hc_aezkh_alt_1;SVTYPE=DEL;EXPERIMENT=1;SAMPLESET=1;END=429419;REGION=nsv2781690;AC=124;AF=0.279;AN=444
chr2L602308nssv13657624T..DBVARID;CALLID=chr2L_hc_tnyhg_alt_1;SVTYPE=DEL;EXPERIMENT=1;SAMPLESET=1;END=602362;REGION=nsv2781053;AC=56;AF=0.126;AN=444
chr2L609345nssv13657429T..DBVARID;CALLID=chr2L_hc_iaujd_alt_1;SVTYPE=DEL;EXPERIMENT=1;SAMPLESET=1;END=609408;REGION=nsv2781000;AC=67;AF=0.151;AN=444
chr2L666211nssv13657616G..DBVARID;CALLID=chr2L_hc_tdwxu_alt_1;SVTYPE=INS;EXPERIMENT=1;SAMPLESET=1;END=666211;REGION=nsv2781423;AC=68;AF=0.153;AN=444
chr2L795312nssv13657500G..DBVARID;CALLID=chr2L_hc_msajw_alt_1;SVTYPE=DEL;EXPERIMENT=1;SAMPLESET=1;END=795369;REGION=nsv2779663;AC=95;AF=0.214;AN=444
chr2L811082nssv13657714T..DBVARID;CALLID=chr2L_hc_yztgb_alt_1;SVTYPE=DEL;EXPERIMENT=1;SAMPLESET=1;END=811203;REGION=nsv2780795;AC=1;AF=0.002252;AN=444

dbVar (dbvar) Track Description
 

Description

These tracks show the locations of large structural variations in the D. melanogaster genome from the NCBI dbVar database. The datasets were obtained from the NCBI FTP site, and they include the results from the following studies:

AccessionManuscript
nstd25 Dopman EB, Hartl DL. A portrait of copy-number polymorphism in Drosophila melanogaster. Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):19920-5.
nstd26 Emerson JJ, Cardoso-Moreira M, Borevitz JO, Long M. Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster. Science. 2008 Jun 20;320(5883):1629-31.
estd205 Zichner T, Garfield DA, Rausch T, Stütz AM, Cannavó E, Braun M, Furlong EE, Korbel JO. Impact of genomic structural variation in Drosophila melanogaster based on population-scale sequencing. Genome Res. 2013 Mar;23(3):568-79.
nstd134 Gilks WP, Pennell TM, Flis I, Webster MT, Morrow EH. Whole genome resequencing of a laboratory-adapted Drosophila melanogaster population sample. Version 3. F1000Res. 2016 Nov 7 [revised 2016 Dec 22];5:2644.

References

Lappalainen I, Lopez J, Skipper L, Hefferon T, Spalding JD, Garner J, Chen C, Maguire M, Corbett M, Zhou G, Paschall J, Ananiev V, Flicek P, Church DM. DbVar and DGVa: public archives for genomic structural variation. Nucleic Acids Res. 2013 Jan;41(Database issue):D936-41.