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nsv5493165

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,131

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 606 SVs from 71 studies. See in: genome view    
Submitted genomic137,273,280-137,294,410Question Mark
Overlapping variant regions from other studies: 606 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):140,167,732-140,188,862Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5493165Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9137,273,280137,294,410
nsv5493165RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9140,167,732140,188,862

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17029653duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17029653Submitted genomicNC_000009.12:g.137
273280_137294410du
p
GRCh38 (hg38)NC_000009.12Chr9137,273,280137,294,410
nssv17029653RemappedPerfectNC_000009.11:g.140
167732_140188862du
p
GRCh37.p13First PassNC_000009.11Chr9140,167,732140,188,862

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)
nssv170296530.00196402
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