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nsv5402855

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 22 studies. See in: genome view    
Submitted genomic111,751,548-111,751,592Question Mark
Overlapping variant regions from other studies: 96 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):114,513,828-114,513,872Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402855Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9111,751,548111,751,592
nsv5402855RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9114,513,828114,513,872

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028288alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028288Submitted genomicNC_000009.12:g.111
751548_111751592in
s281
GRCh38 (hg38)NC_000009.12Chr9111,751,548111,751,592
nssv17028288RemappedPerfectNC_000009.11:g.114
513828_114513872in
s281
GRCh37.p13First PassNC_000009.11Chr9114,513,828114,513,872

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)
nssv17028288<0.00116404
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