A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799621



Internal ID19161050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22710298..22761937hg38UCSC Ensembl
Innerchr14:23179507..23231146hg19UCSC Ensembl
Innerchr14:22249347..22300986hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3851640
hg1951640
hg1851640
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892473
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799621
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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