A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791514



Internal ID18823399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7587317..7876057hg38UCSC Ensembl
Innerchr20:7567964..7856704hg19UCSC Ensembl
Innerchr20:7515964..7804704hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38288741
hg19288741
hg18288741
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893279
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791514
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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