A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25795867



Internal ID19168756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68539099..68612606hg38UCSC Ensembl
Innerchr4:69404817..69478324hg19UCSC Ensembl
Innerchr4:69087412..69160919hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3873508
hg1973508
hg1873508
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893940
Supporting Variants
Samples
Known GenesUGT2B17
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25795867
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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