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nsv5484627

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view    
Submitted genomic117,514,488-117,514,550Question Mark
Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):117,154,542-117,154,604Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5484627Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7117,514,488117,514,550
nsv5484627RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7117,154,542117,154,604

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001687deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001687Submitted genomicNC_000007.14:g.117
514488_117514550de
l
GRCh38 (hg38)NC_000007.14Chr7117,514,488117,514,550
nssv17001687RemappedPerfectNC_000007.13:g.117
154542_117154604de
l
GRCh37.p13First PassNC_000007.13Chr7117,154,542117,154,604

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)
nssv17001687<0.00116404
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