A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789107



Internal ID19180236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62167862..62273374hg38UCSC Ensembl
Innerchr14:62634580..62740092hg19UCSC Ensembl
Innerchr14:61704333..61809845hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38105513
hg19105513
hg18105513
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892553
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789107
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