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nsv5483867

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,912

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 149 SVs from 31 studies. See in: genome view    
Submitted genomic117,645,591-117,650,502Question Mark
Overlapping variant regions from other studies: 149 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):117,285,645-117,290,556Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483867Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7117,645,591117,650,502
nsv5483867RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7117,285,645117,290,556

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001702deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001702Submitted genomicNC_000007.14:g.117
645591_117650502de
l
GRCh38 (hg38)NC_000007.14Chr7117,645,591117,650,502
nssv17001702RemappedPerfectNC_000007.13:g.117
285645_117290556de
l
GRCh37.p13First PassNC_000007.13Chr7117,285,645117,290,556

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)
nssv17001702<0.00156404
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