A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893005



Internal ID18837139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36168874..36215910hg38UCSC Ensembl
Outerchr17:36153146..36215910hg38UCSC Ensembl
Innerchr17:34496232..34543364hg19UCSC Ensembl
Outerchr17:34480526..34543364hg19UCSC Ensembl
Innerchr17:31520345..31567477hg18UCSC Ensembl
Outerchr17:31504639..31567477hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3862765
hg1962839
hg1862839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778304, essv25787004, essv25801144, essv25786650
Samples
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2, TBC1D3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893005
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer