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nsv5965062

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,183,884

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2726 SVs from 86 studies. See in: genome view    
Submitted genomic29,285,033-30,468,916Question Mark
Overlapping variant regions from other studies: 7009 SVs from 116 studies. See in: genome view    
Remapped(Score: Pass):190,198,664-190,843,361Question Mark
Overlapping variant regions from other studies: 3539 SVs from 102 studies. See in: genome view    
Remapped(Score: Pass):25,864,401-29,615,130Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5965062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2029,285,03330,468,916
nsv5965062RemappedPassGRCh37.p13Primary AssemblySecond PassNC_000004.11Chr4190,198,664190,843,361
nsv5965062RemappedPassGRCh37.p13Primary AssemblySecond PassNC_000020.10Chr2025,864,40129,615,130

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17403133deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17403133Submitted genomicNC_000020.11:g.292
85033_30468916del
GRCh38 (hg38)NC_000020.11Chr2029,285,03330,468,916
nssv17403133RemappedPassNC_000004.11:g.190
198664_190843361de
lNC_000020.10:g.25
864401_29615130del
GRCh37.p13Second PassNC_000004.11Chr4190,198,664190,843,361
nssv17403133RemappedPassNC_000004.11:g.190
198664_190843361de
lNC_000020.10:g.25
864401_29615130del
GRCh37.p13Second PassNC_000020.10Chr2025,864,40129,615,130

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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