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nsv4177476

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):137,234,048-137,243,048Question Mark
Overlapping variant regions from other studies: 103 SVs from 11 studies. See in: genome view    
Submitted genomic140,128,500-140,137,500Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4177476RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9137,234,048137,243,048
nsv4177476Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr9140,128,500140,137,500

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15987373duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15987373RemappedPerfectNC_000009.12:g.137
234048_137243048du
p
GRCh38.p12First PassNC_000009.12Chr9137,234,048137,243,048
nssv15987373Submitted genomicNC_000009.11:g.140
128500_140137500du
p
GRCh37.p13NC_000009.11Chr9140,128,500140,137,500

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)
nssv159873730.00815319790
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