A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790149



Internal ID19162662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25214652..25388598hg38UCSC Ensembl
Innerchr14:25683858..25857804hg19UCSC Ensembl
Innerchr14:24753698..24927644hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38173947
hg19173947
hg18173947
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892479
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790149
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