A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105697



Internal ID21274876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:1567921..1583780hg38UCSC Ensembl
Innerchr2:1571693..1587552hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3815860
hg1915860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114138
Supporting Variants
Samplessample213
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105697
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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