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nsv4372743

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:302,558

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 919 SVs from 74 studies. See in: genome view    
Remapped(Score: Perfect):137,165,508-137,468,065Question Mark
Overlapping variant regions from other studies: 919 SVs from 74 studies. See in: genome view    
Submitted genomic137,923,078-138,225,635Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4372743RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2137,165,508137,468,065
nsv4372743Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2137,923,078138,225,635

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15645730copy number loss2-0142-001SNP arrayGenotyping21

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15645730RemappedPerfectNC_000002.12:g.(?_
137165508)_(137468
065_?)del
GRCh38.p12First PassNC_000002.12Chr2137,165,508137,468,065
nssv15645730Submitted genomicNC_000002.11:g.(?_
137923078)_(138225
635_?)del
GRCh37 (hg19)NC_000002.11Chr2137,923,078138,225,635

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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