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nsv2741396

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,384,951

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2148 SVs from 83 studies. See in: genome view    
Remapped(Score: Pass):36,034,953-46,419,903Question Mark
Overlapping variant regions from other studies: 2464 SVs from 75 studies. See in: genome view    
Remapped(Score: Pass):35,269,324-46,453,815Question Mark
Overlapping variant regions from other studies: 876 SVs from 23 studies. See in: genome view    
Submitted genomic35,126,825-45,011,316Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2741396RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1636,034,95346,419,903
nsv2741396RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1635,269,32446,453,815
nsv2741396Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000016.8Chr1635,126,82545,011,316

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13566674deletionSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13566674RemappedPassNC_000016.10:g.(?_
36034953)_(4641990
3_?)del
GRCh38.p12First PassNC_000016.10Chr1636,034,95346,419,903
nssv13566674RemappedPassNC_000016.9:g.(?_3
5269324)_(46453815
_?)del
GRCh37.p13First PassNC_000016.9Chr1635,269,32446,453,815
nssv13566674Submitted genomicNC_000016.8:g.(?_3
5126825)_(45011316
_?)del
NCBI36 (hg18)NC_000016.8Chr1635,126,82545,011,316

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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