A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065364



Internal ID18807895
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 StatusM
Merged Variantsdgv4343n100
Supporting Variantsnssv3584457
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)nsv1065364
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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