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nsv5483905

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:335,932

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1394 SVs from 81 studies. See in: genome view    
Submitted genomic129,698,067-130,033,998Question Mark
Overlapping variant regions from other studies: 1394 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):132,460,346-132,796,277Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483905Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9129,698,067130,033,998
nsv5483905RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9132,460,346132,796,277

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028868duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028868Submitted genomicNC_000009.12:g.129
698067_130033998du
p
GRCh38 (hg38)NC_000009.12Chr9129,698,067130,033,998
nssv17028868RemappedPerfectNC_000009.11:g.132
460346_132796277du
p
GRCh37.p13First PassNC_000009.11Chr9132,460,346132,796,277

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)
nssv17028868<0.00126404
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