A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797823



Internal ID19182400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62557214..62592974hg38UCSC Ensembl
Innerchr15:62849413..62885173hg19UCSC Ensembl
Innerchr15:60636705..60672465hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3835761
hg1935761
hg1835761
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892708
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797823
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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