A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891842



Internal ID19186238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66016734..66626755hg38UCSC Ensembl
Outerchr10:66016734..66626755hg38UCSC Ensembl
Innerchr10:67776492..68386513hg19UCSC Ensembl
Outerchr10:67776492..68386513hg19UCSC Ensembl
Innerchr10:67446498..68056519hg18UCSC Ensembl
Outerchr10:67446498..68056519hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38610022
hg19610022
hg18610022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788009
Samples
Known GenesCTNNA3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891842
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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