A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893925



Internal ID19184779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58675801..58771308hg38UCSC Ensembl
Outerchr4:58675801..58771308hg38UCSC Ensembl
Innerchr4:59541966..59637473hg19UCSC Ensembl
Outerchr4:59541966..59637473hg19UCSC Ensembl
Innerchr4:59236723..59332230hg18UCSC Ensembl
Outerchr4:59236723..59332230hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3895508
hg1995508
hg1895508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797352
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893925
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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