A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584941



Internal ID18536536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46051200..46105732hg38UCSC Ensembl
Innerchr20:44679839..44734371hg19UCSC Ensembl
Innerchr20:44113246..44167778hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3854533
hg1954533
hg1854533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063229
Supporting Variants
Samples
Known GenesNCOA5, SLC12A5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584941
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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