A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785716



Internal ID19170774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:72986169..73015964hg38UCSC Ensembl
Innerchr18:70653404..70683199hg19UCSC Ensembl
Innerchr18:68804384..68834179hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3829796
hg1929796
hg1829796
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893143
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785716
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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