A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788167



Internal ID19173645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64709515..65002828hg38UCSC Ensembl
Innerchr13:65283647..65576960hg19UCSC Ensembl
Innerchr13:64181648..64474961hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38293314
hg19293314
hg18293314
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892373
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=65
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788167
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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