A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788888



Internal ID18827035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:415105..743226hg38UCSC Ensembl
Innerchr18:415105..743226hg19UCSC Ensembl
Innerchr18:405105..733226hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38328122
hg19328122
hg18328122
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893055
Supporting Variants
Samples
Known GenesC18orf56, CETN1, CLUL1, COLEC12, ENOSF1, TYMS, YES1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=127
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788888
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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