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nsv5479161

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,979

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 178 SVs from 41 studies. See in: genome view    
Submitted genomic125,188,256-125,210,234Question Mark
Overlapping variant regions from other studies: 178 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):127,950,535-127,972,513Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5479161Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9125,188,256125,210,234
nsv5479161RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9127,950,535127,972,513

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028667duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028667Submitted genomicNC_000009.12:g.125
188256_125210234du
p
GRCh38 (hg38)NC_000009.12Chr9125,188,256125,210,234
nssv17028667RemappedPerfectNC_000009.11:g.127
950535_127972513du
p
GRCh37.p13First PassNC_000009.11Chr9127,950,535127,972,513

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)
nssv17028667<0.00146404
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