A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893716



Internal ID19184536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65233420..65247096hg38UCSC Ensembl
Outerchr3:65233420..65247096hg38UCSC Ensembl
Innerchr3:65219095..65232771hg19UCSC Ensembl
Outerchr3:65219095..65232771hg19UCSC Ensembl
Innerchr3:65194135..65207811hg18UCSC Ensembl
Outerchr3:65194135..65207811hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3813677
hg1913677
hg1813677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788288
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893716
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer