A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792899



Internal ID18816819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36092731..36160457hg38UCSC Ensembl
Innerchr17:34420079..34487830hg19UCSC Ensembl
Innerchr17:31444192..31511943hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3867727
hg1967752
hg1867752
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 HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792899
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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