U.S. flag

An official website of the United States government

nsv4535086

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 35 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):156,346,938-156,346,938Question Mark
Overlapping variant regions from other studies: 36 SVs from 7 studies. See in: genome view    
Submitted genomic156,316,729-156,316,729Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4535086RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1156,346,938156,346,938
nsv4535086Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1156,316,729156,316,729

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16027790insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16027790RemappedPerfectNC_000001.11:g.156
346938_156346939in
s1267
GRCh38.p12First PassNC_000001.11Chr1156,346,938156,346,938
nssv16027790Submitted genomicNC_000001.10:g.156
316729_156316730in
s1267
GRCh37.p13NC_000001.10Chr1156,316,729156,316,729

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)
nssv160277904.6e-005121694
Support Center