A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792037



Internal ID19160537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78830545..78847535hg38UCSC Ensembl
Innerchr18:76590545..76607535hg19UCSC Ensembl
Innerchr18:74691533..74708523hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3816991
hg1916991
hg1816991
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893154
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792037
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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