A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791345



Internal ID18821709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25391998..26039471hg38UCSC Ensembl
Innerchr18:22971962..23619435hg19UCSC Ensembl
Innerchr18:21225960..21873433hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38647474
hg19647474
hg18647474
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893078
Supporting Variants
Samples
Known GenesSS18
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=157
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791345
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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