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nsv5481062

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:238

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
Submitted genomic123,156,434-123,156,671Question Mark
Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):125,918,713-125,918,950Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5481062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9123,156,434123,156,671
nsv5481062RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,918,713125,918,950

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027153duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027153Submitted genomicNC_000009.12:g.123
156434_123156671du
p
GRCh38 (hg38)NC_000009.12Chr9123,156,434123,156,671
nssv17027153RemappedPerfectNC_000009.11:g.125
918713_125918950du
p
GRCh37.p13First PassNC_000009.11Chr9125,918,713125,918,950

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)
nssv17027153<0.00156404
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