A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893926



Internal ID19184780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59609764..59666359hg38UCSC Ensembl
Outerchr4:59609764..59666359hg38UCSC Ensembl
Innerchr4:60475482..60532077hg19UCSC Ensembl
Outerchr4:60475482..60532077hg19UCSC Ensembl
Innerchr4:60158077..60214672hg18UCSC Ensembl
Outerchr4:60158077..60214672hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3856596
hg1956596
hg1856596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787442
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893926
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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