A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585914



Internal ID16373323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32583046..32584411hg38UCSC Ensembl
Innerchr20:31170848..31172213hg19UCSC Ensembl
Innerchr20:30634509..30635874hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381366
hg191366
hg181366
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939258, nssv939259, nssv939260
Samples
Known GenesC20orf112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585914
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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