A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788801



Internal ID18826076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26576250..26626972hg38UCSC Ensembl
Innerchr13:27150387..27201109hg19UCSC Ensembl
Innerchr13:26048387..26099109hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3850723
hg1950723
hg1850723
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892322
Supporting Variants
Samples
Known GenesWASF3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788801
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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