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nsv5492198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,513

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 212 SVs from 43 studies. See in: genome view    
Submitted genomic138,793,156-138,823,668Question Mark
Overlapping variant regions from other studies: 212 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):138,477,901-138,508,413Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5492198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7138,793,156138,823,668
nsv5492198RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7138,477,901138,508,413

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17006306duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17006306Submitted genomicNC_000007.14:g.138
793156_138823668du
p
GRCh38 (hg38)NC_000007.14Chr7138,793,156138,823,668
nssv17006306RemappedPerfectNC_000007.13:g.138
477901_138508413du
p
GRCh37.p13First PassNC_000007.13Chr7138,477,901138,508,413

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)
nssv17006306<0.00146404
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