A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893988



Internal ID19184842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91769911..91962706hg38UCSC Ensembl
Outerchr4:91769911..91962706hg38UCSC Ensembl
Innerchr4:92691062..92883857hg19UCSC Ensembl
Outerchr4:92691062..92883857hg19UCSC Ensembl
Innerchr4:92910085..93102880hg18UCSC Ensembl
Outerchr4:92910085..93102880hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38192796
hg19192796
hg18192796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796207
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893988
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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