A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585286



Internal ID16026009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3747323..3803946hg38UCSC Ensembl
Innerchr20:3727970..3784593hg19UCSC Ensembl
Innerchr20:3675970..3732593hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3856624
hg1956624
hg1856624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937351
Samples
Known GenesC20orf27, CDC25B, CENPB, HSPA12B, SPEF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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