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nsv5475613

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,260

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 27 studies. See in: genome view    
Submitted genomic123,815,221-123,835,480Question Mark
Overlapping variant regions from other studies: 139 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):123,455,275-123,475,534Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5475613Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7123,815,221123,835,480
nsv5475613RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7123,455,275123,475,534

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001526duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001526Submitted genomicNC_000007.14:g.123
815221_123835480du
p
GRCh38 (hg38)NC_000007.14Chr7123,815,221123,835,480
nssv17001526RemappedPerfectNC_000007.13:g.123
455275_123475534du
p
GRCh37.p13First PassNC_000007.13Chr7123,455,275123,475,534

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)
nssv17001526<0.00126404
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