A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584457



Internal ID18536052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62392097..62555115hg38UCSC Ensembl
Innerchr20:60967153..61152322hg19UCSC Ensembl
Innerchr20:60400548..60562767hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38163019
hg19185170
hg18162220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065364
Supporting Variants
Samples
Known GenesC20orf166, C20orf166-AS1, CABLES2, GATA5, MIR1-1, RBBP8NL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584457
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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