A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066416



Internal ID19155635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40947924..41010760hg38UCSC Ensembl
Innerchr20:39576564..39639400hg19UCSC Ensembl
Innerchr20:39009978..39072814hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3862837
hg1962837
hg1862837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584781
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)nsv1066416
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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