A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791079



Internal ID19178521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14194215..14281865hg38UCSC Ensembl
Innerchr18:14194214..14281864hg19UCSC Ensembl
Innerchr18:14184214..14271864hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3887651
hg1987651
hg1887651
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893076
Supporting Variants
Samples
Known GenesANKRD20A5P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791079
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