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nsv5489760

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:264,667

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3649 SVs from 100 studies. See in: genome view    
Submitted genomic11,910,508-12,175,174Question Mark
Overlapping variant regions from other studies: 3653 SVs from 100 studies. See in: genome view    
Remapped(Score: Perfect):11,910,508-12,175,174Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489760Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr911,910,50812,175,174
nsv5489760RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr911,910,50812,175,174

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17022313deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17022313Submitted genomicNC_000009.12:g.119
10508_12175174del
GRCh38 (hg38)NC_000009.12Chr911,910,50812,175,174
nssv17022313RemappedPerfectNC_000009.11:g.119
10508_12175174del
GRCh37.p13First PassNC_000009.11Chr911,910,50812,175,174

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)
nssv17022313<0.00146404
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