A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788161



Internal ID19162870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78463222..78772415hg38UCSC Ensembl
Innerchr9:81078138..81387331hg19UCSC Ensembl
Innerchr9:80267958..80577151hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38309194
hg19309194
hg18309194
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891684
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=71
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788161
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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