A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788682



Internal ID19173044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62167862..62322229hg38UCSC Ensembl
Innerchr14:62634580..62788947hg19UCSC Ensembl
Innerchr14:61704333..61858700hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38154368
hg19154368
hg18154368
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=42
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788682
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