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nsv2745507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,670,381

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 6474 SVs from 103 studies. See in: genome view    
Remapped(Score: Pass):34,283,456-37,953,836Question Mark
Overlapping variant regions from other studies: 5437 SVs from 102 studies. See in: genome view    
Remapped(Score: Pass):34,436,391-38,347,638Question Mark
Overlapping variant regions from other studies: 1838 SVs from 31 studies. See in: genome view    
Submitted genomic34,327,658-36,633,905Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2745507RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1234,283,45637,953,836
nsv2745507RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1234,436,39138,347,638
nsv2745507Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr1234,327,65836,633,905

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13600797deletionSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13600797RemappedPassNC_000012.12:g.(?_
34283456)_(3795383
6_?)del
GRCh38.p12First PassNC_000012.12Chr1234,283,45637,953,836
nssv13600797RemappedPassNC_000012.11:g.(?_
34436391)_(3834763
8_?)del
GRCh37.p13First PassNC_000012.11Chr1234,436,39138,347,638
nssv13600797Submitted genomicNC_000012.10:g.(?_
34327658)_(3663390
5_?)del
NCBI36 (hg18)NC_000012.10Chr1234,327,65836,633,905

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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