A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797818



Internal ID19164660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69070840..69121961hg38UCSC Ensembl
Innerchr13:69644972..69696093hg19UCSC Ensembl
Innerchr13:68542973..68594094hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3851122
hg1951122
hg1851122
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892384
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797818
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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