A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586564



Internal ID16027287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63276267..63321213hg38UCSC Ensembl
Innerchr20:61907619..61952565hg19UCSC Ensembl
Innerchr20:61378064..61423010hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3844947
hg1944947
hg1844947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943744
Samples
Known GenesARFGAP1, COL20A1, MIR4326
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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