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nsv5534602

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,226

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 166 SVs from 41 studies. See in: genome view    
Submitted genomic42,702,618-42,704,843Question Mark
Overlapping variant regions from other studies: 166 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):43,098,624-43,100,849Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5534602Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2242,702,61842,704,843
nsv5534602RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2243,098,62443,100,849

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17729255deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17729255Submitted genomicNC_000022.11:g.427
02618_42704843del
GRCh38 (hg38)NC_000022.11Chr2242,702,61842,704,843
nssv17729255RemappedPerfectNC_000022.10:g.430
98624_43100849del
GRCh37.p13First PassNC_000022.10Chr2243,098,62443,100,849

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)
nssv17729255<0.00126404
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