A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798885



Internal ID19178384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39148850..39293397hg38UCSC Ensembl
Innerchr18:36728814..36873361hg19UCSC Ensembl
Innerchr18:34982812..35127359hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38144548
hg19144548
hg18144548
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893089
Supporting Variants
Samples
Known GenesLINC00669
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798885
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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