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nsv5483490

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:416

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 47 studies. See in: genome view    
Submitted genomic134,665,255-134,665,670Question Mark
Overlapping variant regions from other studies: 144 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):134,350,007-134,350,422Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483490Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7134,665,255134,665,670
nsv5483490RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7134,350,007134,350,422

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17003636deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17003636Submitted genomicNC_000007.14:g.134
665255_134665670de
l
GRCh38 (hg38)NC_000007.14Chr7134,665,255134,665,670
nssv17003636RemappedPerfectNC_000007.13:g.134
350007_134350422de
l
GRCh37.p13First PassNC_000007.13Chr7134,350,007134,350,422

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)
nssv170036360.56736346404
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