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nsv5561314

  • 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: 102 SVs from 20 studies. See in: genome view    
Submitted genomic156,752,879-156,752,930Question Mark
Overlapping variant regions from other studies: 108 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):156,722,671-156,722,722Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1156,752,879156,752,930
nsv5561314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1156,722,671156,722,722

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890921sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890921Submitted genomicNC_000001.11:g.156
752879_156752930in
s316
GRCh38 (hg38)NC_000001.11Chr1156,752,879156,752,930
nssv16890921RemappedPerfectNC_000001.10:g.156
722671_156722722in
s316
GRCh37.p13First PassNC_000001.10Chr1156,722,671156,722,722

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)
nssv16890921<0.00116404
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