A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939258



Internal ID16233214
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585914
Supporting Variants
Samples
Known GenesC20orf112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939258
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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