A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893633



Internal ID18837767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3989971..4029467hg38UCSC Ensembl
Outerchr3:3989971..4036970hg38UCSC Ensembl
Innerchr3:4031655..4071151hg19UCSC Ensembl
Outerchr3:4031655..4078654hg19UCSC Ensembl
Innerchr3:4006655..4046151hg18UCSC Ensembl
Outerchr3:4006655..4053654hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3847000
hg1947000
hg1847000
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785434, essv25791115
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893633
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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