A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788047



Internal ID18831855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37244892..37513971hg38UCSC Ensembl
Innerchr13:37819029..38088108hg19UCSC Ensembl
Innerchr13:36717029..36986108hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38269080
hg19269080
hg18269080
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892331
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=66
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788047
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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