A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891810



Internal ID19186206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52943795..53164852hg38UCSC Ensembl
Outerchr10:52940107..53171210hg38UCSC Ensembl
Innerchr10:54703555..54924612hg19UCSC Ensembl
Outerchr10:54699867..54930970hg19UCSC Ensembl
Innerchr10:54373561..54594618hg18UCSC Ensembl
Outerchr10:54369873..54600976hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38231104
hg19231104
hg18231104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787760, essv25789843, essv25790444, essv25787861, essv25787828, essv25792421
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891810
Frequency
Sample Size3017
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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