A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064118



Internal ID19153337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12633437..12660724hg38UCSC Ensembl
Innerchr20:12614084..12641371hg19UCSC Ensembl
Innerchr20:12562084..12589371hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3827288
hg1927288
hg1827288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599385
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)nsv1064118
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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