A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106952



Internal ID21287967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32556338..32691009hg38UCSC Ensembl
Innerchr2:32781405..32916076hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38134672
hg19134672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117765
Supporting Variants
Samplessample410
Known GenesBIRC6, MIR4765, TTC27
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106952
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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