A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789968



Internal ID18814424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105680045..106390146hg38UCSC Ensembl
Innerchr14:106146382..106846077hg19UCSC Ensembl
Innerchr14:105217427..105917122hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38710102
hg19699696
hg18699696
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892584
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00226
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=39
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789968
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