A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586537



Internal ID16373946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63093505..63100275hg38UCSC Ensembl
Innerchr20:61724857..61731627hg19UCSC Ensembl
Innerchr20:61195302..61202072hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386771
hg196771
hg186771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942354
Samples
Known GenesHAR1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586537
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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