A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792432



Internal ID19181894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23952256..24295326hg38UCSC Ensembl
Innerchr11:23973802..24316872hg19UCSC Ensembl
Innerchr11:23930378..24273448hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38343071
hg19343071
hg18343071
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891951
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=64
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792432
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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