A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788919



Internal ID19171733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84279764..84391050hg38UCSC Ensembl
Innerchr7:83909080..84020366hg19UCSC Ensembl
Innerchr7:83747016..83858302hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38111287
hg19111287
hg18111287
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891160
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788919
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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