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nsv5476646

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 25 studies. See in: genome view    
Submitted genomic131,556,668-131,556,734Question Mark
Overlapping variant regions from other studies: 112 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):131,241,427-131,241,493Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5476646Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7131,556,668131,556,734
nsv5476646RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7131,241,427131,241,493

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17005212deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17005212Submitted genomicNC_000007.14:g.131
556668_131556734de
l
GRCh38 (hg38)NC_000007.14Chr7131,556,668131,556,734
nssv17005212RemappedPerfectNC_000007.13:g.131
241427_131241493de
l
GRCh37.p13First PassNC_000007.13Chr7131,241,427131,241,493

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)
nssv17005212<0.00126404
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