A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780569



Internal ID19178066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62180723..62244147hg38UCSC Ensembl
Innerchr14:62647441..62710865hg19UCSC Ensembl
Innerchr14:61717194..61780618hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3863425
hg1963425
hg1863425
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892554
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780569
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