A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799326



Internal ID18819455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3899706..4124049hg38UCSC Ensembl
Innerchr3:3941390..4165733hg19UCSC Ensembl
Innerchr3:3916390..4140733hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38224344
hg19224344
hg18224344
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893635
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=93
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799326
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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