A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788911



Internal ID18816129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:17781183..18035151hg38UCSC Ensembl
Innerchr2:17962450..18216417hg19UCSC Ensembl
Innerchr2:17825931..18079898hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38253969
hg19253968
hg18253968
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891603
Supporting Variants
Samples
Known GenesGEN1, KCNS3, MSGN1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=84
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788911
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