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nsv6146348

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:794,518

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 5858 SVs from 121 studies. See in: genome view    
Submitted genomic22,099,191-22,893,708Question Mark
Overlapping variant regions from other studies: 5896 SVs from 121 studies. See in: genome view    
Remapped(Score: Good):22,453,601-23,235,888Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6146348Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2222,099,19122,893,708
nsv6146348RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2222,453,60123,235,888

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17727846deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17727846Submitted genomicNC_000022.11:g.220
99191_22893708del
GRCh38 (hg38)NC_000022.11Chr2222,099,19122,893,708
nssv17727846RemappedGoodNC_000022.10:g.224
53601_23235888del
GRCh37.p13First PassNC_000022.10Chr2222,453,60123,235,888

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)
nssv177278460.0432716372
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