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nsv5483613

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 77 SVs from 18 studies. See in: genome view    
Submitted genomic122,376,093-122,376,156Question Mark
Overlapping variant regions from other studies: 77 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):125,138,372-125,138,435Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483613Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,376,093122,376,156
nsv5483613RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,138,372125,138,435

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027756duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027756Submitted genomicNC_000009.12:g.122
376093_122376156du
p
GRCh38 (hg38)NC_000009.12Chr9122,376,093122,376,156
nssv17027756RemappedPerfectNC_000009.11:g.125
138372_125138435du
p
GRCh37.p13First PassNC_000009.11Chr9125,138,372125,138,435

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)
nssv17027756<0.00116404
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