A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064782



Internal ID19154001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55198442..55330294hg38UCSC Ensembl
Innerchr20:53814981..53946833hg19UCSC Ensembl
Innerchr20:53248388..53380240hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38131853
hg19131853
hg18131853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584231
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064782
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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