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nsv5533140

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,821

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 25 studies. See in: genome view    
Submitted genomic57,210,309-57,212,129Question Mark
Overlapping variant regions from other studies: 96 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):55,785,365-55,787,185Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533140Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2057,210,30957,212,129
nsv5533140RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2055,785,36555,787,185

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17733281deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17733281Submitted genomicNC_000020.11:g.572
10309_57212129del
GRCh38 (hg38)NC_000020.11Chr2057,210,30957,212,129
nssv17733281RemappedPerfectNC_000020.10:g.557
85365_55787185del
GRCh37.p13First PassNC_000020.10Chr2055,785,36555,787,185

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)
nssv17733281<0.00116404
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