A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893997



Internal ID18838165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:101080966..101120892hg38UCSC Ensembl
Outerchr4:101080966..101120892hg38UCSC Ensembl
Innerchr4:102002123..102042049hg19UCSC Ensembl
Outerchr4:102002123..102042049hg19UCSC Ensembl
Innerchr4:102221146..102261072hg18UCSC Ensembl
Outerchr4:102221146..102261072hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3839927
hg1939927
hg1839927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780721
Samples
Known GenesPPP3CA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893997
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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