A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791115



Internal ID18827102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3989971..4036970hg38UCSC Ensembl
Innerchr3:4031655..4078654hg19UCSC Ensembl
Innerchr3:4006655..4053654hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3847000
hg1947000
hg1847000
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893633
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791115
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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