A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104993



Internal ID21266616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:225122422..225124136hg38UCSC Ensembl
Innerchr2:225987139..225988853hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg381715
hg191715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115222
Supporting Variants
Samplessample10
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104993
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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