A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893000



Internal ID18837134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36098851..36131859hg38UCSC Ensembl
Outerchr17:36082427..36168874hg38UCSC Ensembl
Innerchr17:34426245..34459241hg19UCSC Ensembl
Outerchr17:34409784..34496232hg19UCSC Ensembl
Innerchr17:31450358..31483354hg18UCSC Ensembl
Outerchr17:31433897..31520345hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3886448
hg1986449
hg1886449
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782315, essv25788433, essv25789306, essv25789748, essv25787942, essv25788666, essv25785011, essv25789054, essv25785986, essv25792899, essv25791006, essv25788004, essv25788072, essv25788181, essv25788077, essv25788994, essv25787829, essv25788197, essv25789017, essv25788028
Samples
Known GenesCCL3, CCL4, TBC1D3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893000
Frequency
Sample Size3017
Observed Gain17
Observed Loss3
Observed Complex0
Frequencyn/a


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