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nsv832424

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:191,692

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 647 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):55,881,442-56,073,133Question Mark
Overlapping variant regions from other studies: 647 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):56,275,226-56,466,917Question Mark
Overlapping variant regions from other studies: 18 SVs from 4 studies. See in: genome view    
Submitted genomic54,561,493-54,753,184Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv832424RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1255,881,44256,073,133
nsv832424RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,275,22656,466,917
nsv832424Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000012.9Chr1254,561,49354,753,184

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1449855copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1449855RemappedPerfectNC_000012.12:g.(55
881442_?)_(?_56073
133)del
GRCh38.p12First PassNC_000012.12Chr1255,881,44256,073,133
nssv1449855RemappedPerfectNC_000012.11:g.(56
275226_?)_(?_56466
917)del
GRCh37.p13First PassNC_000012.11Chr1256,275,22656,466,917
nssv1449855Submitted genomicNC_000012.9:g.(545
61493_?)_(?_547531
84)del
NCBI35 (hg17)NC_000012.9Chr1254,561,49354,753,184

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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