A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894026



Internal ID19184880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:125056854..125166495hg38UCSC Ensembl
Outerchr4:125056854..125166495hg38UCSC Ensembl
Innerchr4:125978009..126087650hg19UCSC Ensembl
Outerchr4:125978009..126087650hg19UCSC Ensembl
Innerchr4:126197459..126307100hg18UCSC Ensembl
Outerchr4:126197459..126307100hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38109642
hg19109642
hg18109642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796875
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894026
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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