A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584229



Internal ID18882510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55130423..55165844hg38UCSC Ensembl
Innerchr20:53746962..53782383hg19UCSC Ensembl
Innerchr20:53180369..53215790hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3835422
hg1935422
hg1835422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060042
Supporting Variants
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)nssv3584229
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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