A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780278



Internal ID19162909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40113931..40127909hg38UCSC Ensembl
Innerchr18:37693895..37707873hg19UCSC Ensembl
Innerchr18:35947893..35961871hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3813979
hg1913979
hg1813979
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893090
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780278
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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