A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787829



Internal ID18823590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36087568..36131859hg38UCSC Ensembl
Innerchr17:34414914..34459241hg19UCSC Ensembl
Innerchr17:31439027..31483354hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3844292
hg1944328
hg1844328
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893000
Supporting Variants
Samples
Known GenesCCL3, CCL4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787829
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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