A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787442



Internal ID19174079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59609764..59666359hg38UCSC Ensembl
Innerchr4:60475482..60532077hg19UCSC Ensembl
Innerchr4:60158077..60214672hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3856596
hg1956596
hg1856596
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893926
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787442
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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