A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939265



Internal ID16233221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32583197..32585037hg38UCSC Ensembl
Innerchr20:31170999..31172839hg19UCSC Ensembl
Innerchr20:30634660..30636500hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381841
hg191841
hg181841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585917
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)nssv939265
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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