A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584516



Internal ID18882797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64242894..64284703hg38UCSC Ensembl
Innerchr20:62874247..62916056hg19UCSC Ensembl
Innerchr20:62344691..62386500hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3841810
hg1941810
hg1841810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055633
Supporting Variants
Samples
Known GenesPCMTD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584516
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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