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nsv5518568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:824

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 22 studies. See in: genome view    
Submitted genomic34,291,533-34,292,356Question Mark
Overlapping variant regions from other studies: 154 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):32,879,339-32,880,162Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2034,291,53334,292,356
nsv5518568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2032,879,33932,880,162

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732088deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732088Submitted genomicNC_000020.11:g.342
91533_34292356del
GRCh38 (hg38)NC_000020.11Chr2034,291,53334,292,356
nssv17732088RemappedPerfectNC_000020.10:g.328
79339_32880162del
GRCh37.p13First PassNC_000020.10Chr2032,879,33932,880,162

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)
nssv17732088<0.00146404
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