A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788004



Internal ID18822210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36087568..36147750hg38UCSC Ensembl
Innerchr17:34414914..34475131hg19UCSC Ensembl
Innerchr17:31439027..31499244hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3860183
hg1960218
hg1860218
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=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788004
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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