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nsv5489736

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:336

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 252 SVs from 36 studies. See in: genome view    
Submitted genomic11,739,422-11,739,757Question Mark
Overlapping variant regions from other studies: 252 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):11,596,931-11,597,266Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489736Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr811,739,42211,739,757
nsv5489736RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr811,596,93111,597,266

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17008315deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17008315Submitted genomicNC_000008.11:g.117
39422_11739757del
GRCh38 (hg38)NC_000008.11Chr811,739,42211,739,757
nssv17008315RemappedPerfectNC_000008.10:g.115
96931_11597266del
GRCh37.p13First PassNC_000008.10Chr811,596,93111,597,266

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)
nssv170083150.0472906390
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