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nsv5910429

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,295,836

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 8978 SVs from 121 studies. See in: genome view    
Submitted genomic34,050,005-38,345,840Question Mark
Overlapping variant regions from other studies: 8145 SVs from 120 studies. See in: genome view    
Remapped(Score: Pass):34,202,940-38,739,642Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5910429Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1234,050,00538,345,840
nsv5910429RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1234,202,94038,739,642

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17357675deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17357675Submitted genomicNC_000012.12:g.340
50005_38345840del
GRCh38 (hg38)NC_000012.12Chr1234,050,00538,345,840
nssv17357675RemappedPassNC_000012.11:g.342
02940_38739642del
GRCh37.p13First PassNC_000012.11Chr1234,202,94038,739,642

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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