A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586366



Internal ID16373775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58890789..58893423hg38UCSC Ensembl
Innerchr20:57465844..57468478hg19UCSC Ensembl
Innerchr20:56899239..56901873hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg382635
hg192635
hg182635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7626n54
Supporting Variantsnssv941810
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586366
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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