A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893055



Internal ID18837189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:511960..706589hg38UCSC Ensembl
Outerchr18:415105..743226hg38UCSC Ensembl
Innerchr18:511960..706589hg19UCSC Ensembl
Outerchr18:415105..743226hg19UCSC Ensembl
Innerchr18:501960..696589hg18UCSC Ensembl
Outerchr18:405105..733226hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38328122
hg19328122
hg18328122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788888, essv25789383
Samples
Known GenesC18orf56, CETN1, CLUL1, COLEC12, ENOSF1, TYMS, YES1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893055
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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