A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787942



Internal ID18813456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36092731..36147750hg38UCSC Ensembl
Innerchr17:34420079..34475131hg19UCSC Ensembl
Innerchr17:31444192..31499244hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3855020
hg1955053
hg1855053
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893000
Supporting Variants
Samples
Known GenesCCL4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787942
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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