A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106030



Internal ID21279779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38375735..38380874hg38UCSC Ensembl
Innerchr2:38602877..38608016hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg385140
hg195140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112054
Supporting Variants
Samplessample289
Known GenesATL2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106030
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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