A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065189



Internal ID18807720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33597378..33807579hg38UCSC Ensembl
Innerchr20:32185184..32395385hg19UCSC Ensembl
Innerchr20:31648845..31859046hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38210202
hg19210202
hg18210202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584743
Samples
Known GenesACTL10, C20orf144, CBFA2T2, E2F1, NECAB3, PXMP4, ZNF341
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065189
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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