A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106353



Internal ID21284252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:29113026..29118458hg38UCSC Ensembl
Innerchr2:29335892..29341324hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg385433
hg195433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112649
Supporting Variants
Samplessample359
Known GenesCLIP4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106353
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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