A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791304



Internal ID19182338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26104702..26320138hg38UCSC Ensembl
Innerchr20:26085338..26300774hg19UCSC Ensembl
Innerchr20:26033338..26248774hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38215437
hg19215437
hg18215437
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893328
Supporting Variants
Samples
Known GenesLOC284801, MIR663A, NCOR1P1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791304
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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