A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781185



Internal ID19177529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73955809..73966933hg38UCSC Ensembl
Innerchr18:71623044..71634168hg19UCSC Ensembl
Innerchr18:69774024..69785148hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3811125
hg1911125
hg1811125
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893150
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781185
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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