A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787760



Internal ID19169684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52940107..53164852hg38UCSC Ensembl
Innerchr10:54699867..54924612hg19UCSC Ensembl
Innerchr10:54369873..54594618hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38224746
hg19224746
hg18224746
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891810
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=57
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787760
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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