A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939358



Internal ID16233314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38377270..38386275hg38UCSC Ensembl
Innerchr20:37005912..37014917hg19UCSC Ensembl
Innerchr20:36439326..36448331hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389006
hg199006
hg189006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585966
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939358
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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