A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801144



Internal ID18820921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36168874..36215910hg38UCSC Ensembl
Innerchr17:34496232..34543364hg19UCSC Ensembl
Innerchr17:31520345..31567477hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3847037
hg1947133
hg1847133
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893005
Supporting Variants
Samples
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2, TBC1D3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801144
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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