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nsv469804

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:166,454

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 487 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):151,547,915-151,714,368Question Mark
Overlapping variant regions from other studies: 487 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):152,404,429-152,570,882Question Mark
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view    
Submitted genomic152,606,974-152,773,427Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469804RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2151,547,915151,714,368
nsv469804RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2152,404,429152,570,882
nsv469804Submitted genomicNCBI34 (hg16)Primary AssemblyGPC_000000200.1Chr2152,606,974152,773,427

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1675031copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1675031RemappedPerfectNC_000002.12:g.(?_
151547915)_(151714
368_?)del
GRCh38.p12First PassNC_000002.12Chr2151,547,915151,714,368
nssv1675031RemappedPerfectNC_000002.11:g.(?_
152404429)_(152570
882_?)del
GRCh37.p13First PassNC_000002.11Chr2152,404,429152,570,882
nssv1675031Submitted genomicGPC_000000200.1:g.
(?_152606974)_(152
773427_?)del
NCBI34 (hg16)GPC_000000200.1Chr2152,606,974152,773,427

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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