A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066814



Internal ID18809345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47342953..47580758hg38UCSC Ensembl
Innerchr20:45971697..46209502hg19UCSC Ensembl
Innerchr20:45405104..45642909hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38237806
hg19237806
hg18237806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731361
Samples
Known GenesNCOA3, ZMYND8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066814
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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