U.S. flag

An official website of the United States government

nsv5400630

  • 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: 97 SVs from 23 studies. See in: genome view    
Submitted genomic115,073,178-115,073,229Question Mark
Overlapping variant regions from other studies: 97 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):117,835,457-117,835,508Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400630Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9115,073,178115,073,229
nsv5400630RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9117,835,457117,835,508

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027803alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027803Submitted genomicNC_000009.12:g.115
073178_115073229in
s281
GRCh38 (hg38)NC_000009.12Chr9115,073,178115,073,229
nssv17027803RemappedPerfectNC_000009.11:g.117
835457_117835508in
s281
GRCh37.p13First PassNC_000009.11Chr9117,835,457117,835,508

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)
nssv17027803<0.00126404
Support Center