A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790982



Internal ID19179130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78463222..78779050hg38UCSC Ensembl
Innerchr9:81078138..81393966hg19UCSC Ensembl
Innerchr9:80267958..80583786hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38315829
hg19315829
hg18315829
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 HumanHap 610
CommentsNumber of probes=78
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790982
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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