A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792655



Internal ID19182672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81176512..81608694hg38UCSC Ensembl
Innerchr7:80805828..81238010hg19UCSC Ensembl
Innerchr7:80643764..81075946hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38432183
hg19432183
hg18432183
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891153
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=77
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792655
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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