A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892708



Internal ID19183528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62566140..62592974hg38UCSC Ensembl
Outerchr15:62557214..62592974hg38UCSC Ensembl
Innerchr15:62858339..62885173hg19UCSC Ensembl
Outerchr15:62849413..62885173hg19UCSC Ensembl
Innerchr15:60645631..60672465hg18UCSC Ensembl
Outerchr15:60636705..60672465hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3835761
hg1935761
hg1835761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797823, essv25797149
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892708
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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