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nsv5516468

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:314

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 164 SVs from 45 studies. See in: genome view    
Submitted genomic34,528,026-34,528,339Question Mark
Overlapping variant regions from other studies: 164 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):33,115,831-33,116,144Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5516468Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2034,528,02634,528,339
nsv5516468RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2033,115,83133,116,144

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732104deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732104Submitted genomicNC_000020.11:g.345
28026_34528339del
GRCh38 (hg38)NC_000020.11Chr2034,528,02634,528,339
nssv17732104RemappedPerfectNC_000020.10:g.331
15831_33116144del
GRCh37.p13First PassNC_000020.10Chr2033,115,83133,116,144

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)
nssv177321040.44628536404
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