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nsv5476659

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:195

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 73 SVs from 17 studies. See in: genome view    
Submitted genomic122,229,067-122,229,261Question Mark
Overlapping variant regions from other studies: 73 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):124,991,346-124,991,540Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5476659Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,229,067122,229,261
nsv5476659RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9124,991,346124,991,540

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027750deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027750Submitted genomicNC_000009.12:g.122
229067_122229261de
l
GRCh38 (hg38)NC_000009.12Chr9122,229,067122,229,261
nssv17027750RemappedPerfectNC_000009.11:g.124
991346_124991540de
l
GRCh37.p13First PassNC_000009.11Chr9124,991,346124,991,540

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)
nssv17027750<0.00116404
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