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nsv5398974

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 18 studies. See in: genome view    
Submitted genomic109,176,826-109,176,877Question Mark
Overlapping variant regions from other studies: 91 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):111,939,106-111,939,157Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5398974Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9109,176,826109,176,877
nsv5398974RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9111,939,106111,939,157

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17026702alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17026702Submitted genomicNC_000009.12:g.109
176826_109176877in
s280
GRCh38 (hg38)NC_000009.12Chr9109,176,826109,176,877
nssv17026702RemappedPerfectNC_000009.11:g.111
939106_111939157in
s280
GRCh37.p13First PassNC_000009.11Chr9111,939,106111,939,157

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)
nssv17026702<0.00116404
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