A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892556



Internal ID19183376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65145330..65205229hg38UCSC Ensembl
Outerchr14:65145330..65205229hg38UCSC Ensembl
Innerchr14:65612048..65671947hg19UCSC Ensembl
Outerchr14:65612048..65671947hg19UCSC Ensembl
Innerchr14:64681801..64741700hg18UCSC Ensembl
Outerchr14:64681801..64741700hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3859900
hg1959900
hg1859900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788156
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892556
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