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nsv5519676

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:479

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 21 studies. See in: genome view    
Submitted genomic34,290,940-34,291,418Question Mark
Overlapping variant regions from other studies: 153 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):32,878,746-32,879,224Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5519676Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2034,290,94034,291,418
nsv5519676RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2032,878,74632,879,224

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732087deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732087Submitted genomicNC_000020.11:g.342
90940_34291418del
GRCh38 (hg38)NC_000020.11Chr2034,290,94034,291,418
nssv17732087RemappedPerfectNC_000020.10:g.328
78746_32879224del
GRCh37.p13First PassNC_000020.10Chr2032,878,74632,879,224

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)
nssv17732087<0.00146404
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