A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782500



Internal ID19175251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69167846..69235288hg38UCSC Ensembl
Innerchr18:66835083..66902525hg19UCSC Ensembl
Innerchr18:64986063..65053505hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3867443
hg1967443
hg1867443
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893132
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782500
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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