A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586074



Internal ID18884355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:51917700..51951569hg38UCSC Ensembl
Innerchr20:50534239..50568108hg19UCSC Ensembl
Innerchr20:49967646..50001515hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3833870
hg1933870
hg1833870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061391
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)nssv3586074
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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