nsv5532672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,613

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 22 studies. See in: genome view    
Submitted genomic2,123,202-2,125,814Question Mark
Overlapping variant regions from other studies: 91 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):2,103,848-2,106,460Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5532672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr202,123,2022,125,814
nsv5532672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr202,103,8482,106,460

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17730302deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17730302Submitted genomicNC_000020.11:g.212
3202_2125814del
GRCh38 (hg38)NC_000020.11Chr202,123,2022,125,814
nssv17730302RemappedPerfectNC_000020.10:g.210
3848_2106460del
GRCh37.p13First PassNC_000020.10Chr202,103,8482,106,460

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)
nssv17730302<0.00116404
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