A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585952



Internal ID16373361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37061383..37087948hg38UCSC Ensembl
Innerchr20:35689786..35716351hg19UCSC Ensembl
Innerchr20:35123200..35149765hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3826566
hg1926566
hg1826566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939349
Samples
Known GenesRBL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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