U.S. flag

An official website of the United States government

nsv4187516

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:355,020

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 405 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):54,898,740-55,253,759Question Mark
Overlapping variant regions from other studies: 405 SVs from 21 studies. See in: genome view    
Submitted genomic56,658,500-57,013,519Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4187516RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1054,898,74055,253,759
nsv4187516Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr1056,658,50057,013,519

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15794109deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15794109RemappedPerfectNC_000010.11:g.548
98740_55253759del
GRCh38.p12First PassNC_000010.11Chr1054,898,74055,253,759
nssv15794109Submitted genomicNC_000010.10:g.566
58500_57013519del
GRCh37.p13NC_000010.10Chr1056,658,50057,013,519

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv157941099.2e-005221694
Support Center