A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586696



Internal ID16374105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63958024..63966082hg38UCSC Ensembl
Innerchr20:62589377..62597435hg19UCSC Ensembl
Innerchr20:62059821..62067879hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388059
hg198059
hg188059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944022
Samples
Known GenesZNF512B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586696
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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