A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787970



Internal ID18820762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76659664..76918686hg38UCSC Ensembl
Innerchr7:76288981..76548003hg19UCSC Ensembl
Innerchr7:76126917..76385939hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38259023
hg19259023
hg18259023
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891147
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787970
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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