A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788009



Internal ID19160671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66016734..66626755hg38UCSC Ensembl
Innerchr10:67776492..68386513hg19UCSC Ensembl
Innerchr10:67446498..68056519hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38610022
hg19610022
hg18610022
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891842
Supporting Variants
Samples
Known GenesCTNNA3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=157
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788009
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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