A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786806



Internal ID18835754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:50871431..50953868hg38UCSC Ensembl
Innerchr18:48397801..48480238hg19UCSC Ensembl
Innerchr18:46651799..46734236hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3882438
hg1982438
hg1882438
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893102
Supporting Variants
Samples
Known GenesME2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786806
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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