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nsv2744527

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,635,530

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 6197 SVs from 102 studies. See in: genome view    
Remapped(Score: Pass):34,283,456-37,918,985Question Mark
Overlapping variant regions from other studies: 5160 SVs from 101 studies. See in: genome view    
Remapped(Score: Pass):34,436,391-38,312,787Question Mark
Overlapping variant regions from other studies: 1801 SVs from 31 studies. See in: genome view    
Submitted genomic34,327,658-36,599,054Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2744527RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1234,283,45637,918,985
nsv2744527RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1234,436,39138,312,787
nsv2744527Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr1234,327,65836,599,054

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13599853deletionSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13599853RemappedPassNC_000012.12:g.(?_
34283456)_(3791898
5_?)del
GRCh38.p12First PassNC_000012.12Chr1234,283,45637,918,985
nssv13599853RemappedPassNC_000012.11:g.(?_
34436391)_(3831278
7_?)del
GRCh37.p13First PassNC_000012.11Chr1234,436,39138,312,787
nssv13599853Submitted genomicNC_000012.10:g.(?_
34327658)_(3659905
4_?)del
NCBI36 (hg18)NC_000012.10Chr1234,327,65836,599,054

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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