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nsv2783850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:352,340

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1269 SVs from 84 studies. See in: genome view    
Remapped(Score: Perfect):53,636,473-53,988,812Question Mark
Overlapping variant regions from other studies: 1274 SVs from 84 studies. See in: genome view    
Remapped(Score: Perfect):55,396,233-55,748,572Question Mark
Overlapping variant regions from other studies: 486 SVs from 25 studies. See in: genome view    
Submitted genomic55,066,239-55,418,578Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2783850RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1053,636,47353,988,812
nsv2783850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1055,396,23355,748,572
nsv2783850Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000010.9Chr1055,066,23955,418,578

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv13662143copy number lossCGPQ-1441SNP arrayGenotyping43

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13662143RemappedPerfectNC_000010.11:g.(?_
53636473)_(5398881
2_?)del
GRCh38.p12First PassNC_000010.11Chr1053,636,47353,988,812
nssv13662143RemappedPerfectNC_000010.10:g.(?_
55396233)_(5574857
2_?)del
GRCh37.p13First PassNC_000010.10Chr1055,396,23355,748,572
nssv13662143Submitted genomicNC_000010.9:g.(?_5
5066239)_(55418578
_?)del
NCBI36 (hg18)NC_000010.9Chr1055,066,23955,418,578

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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