A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063787



Internal ID19153006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14360553..14427444hg38UCSC Ensembl
Innerchr20:14341199..14408090hg19UCSC Ensembl
Innerchr20:14289199..14356090hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3866892
hg1966892
hg1866892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599404
Samples
Known GenesMACROD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063787
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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