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nsv4055085

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,585

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 35 SVs from 9 studies. See in: genome view    
Remapped(Score: Perfect):62,508,720-62,534,304Question Mark
Overlapping variant regions from other studies: 35 SVs from 9 studies. See in: genome view    
Submitted genomic62,735,855-62,761,439Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4055085RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr262,508,72062,534,304
nsv4055085Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr262,735,85562,761,439

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15870363deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15870363RemappedPerfectNC_000002.12:g.625
08720_62534304del
GRCh38.p12First PassNC_000002.12Chr262,508,72062,534,304
nssv15870363Submitted genomicNC_000002.11:g.627
35855_62761439del
GRCh37.p13NC_000002.11Chr262,735,85562,761,439

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)
nssv15870363<0.001521694
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