A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv944741



Internal ID16238697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64315531..64333832hg38UCSC Ensembl
Innerchr20:62946884..62965185hg19UCSC Ensembl
Innerchr20:62417328..62435629hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3818302
hg1918302
hg1818302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586864
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)nssv944741
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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