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nsv2765589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,348,699

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 5594 SVs from 96 studies. See in: genome view    
Remapped(Score: Pass):34,673,639-38,022,337Question Mark
Overlapping variant regions from other studies: 4557 SVs from 95 studies. See in: genome view    
Submitted genomic34,826,574-38,416,139Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2765589RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1234,673,63938,022,337
nsv2765589Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1234,826,57438,416,139

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13545958deletionSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13545958RemappedPassNC_000012.12:g.(?_
34673639)_(3802233
7_?)del
GRCh38.p12First PassNC_000012.12Chr1234,673,63938,022,337
nssv13545958Submitted genomicNC_000012.11:g.(?_
34826574)_(3841613
9_?)del
GRCh37 (hg19)NC_000012.11Chr1234,826,57438,416,139

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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