A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584641



Internal ID18882922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18216088..18287373hg38UCSC Ensembl
Innerchr20:18196732..18268017hg19UCSC Ensembl
Innerchr20:18144732..18216017hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3871286
hg1971286
hg1871286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060123
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584641
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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