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nsv5396659

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 26 studies. See in: genome view    
Submitted genomic111,781,847-111,781,882Question Mark
Overlapping variant regions from other studies: 102 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):114,544,127-114,544,162Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5396659Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9111,781,847111,781,882
nsv5396659RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9114,544,127114,544,162

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028290alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028290Submitted genomicNC_000009.12:g.111
781847_111781882in
s274
GRCh38 (hg38)NC_000009.12Chr9111,781,847111,781,882
nssv17028290RemappedPerfectNC_000009.11:g.114
544127_114544162in
s274
GRCh37.p13First PassNC_000009.11Chr9114,544,127114,544,162

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)
nssv170282900.006406404
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