A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787696



Internal ID18825515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4151816..4283616hg38UCSC Ensembl
Innerchr3:4193500..4325300hg19UCSC Ensembl
Innerchr3:4168500..4300300hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38131801
hg19131801
hg18131801
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893631
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787696
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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