A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783593



Internal ID19168264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68539099..68647187hg38UCSC Ensembl
Innerchr4:69404817..69512905hg19UCSC Ensembl
Innerchr4:69087412..69195500hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38108089
hg19108089
hg18108089
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893940
Supporting Variants
Samples
Known GenesUGT2B15, UGT2B17
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783593
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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