A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893329



Internal ID19184149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26145712..26265450hg38UCSC Ensembl
Outerchr20:26145712..26265450hg38UCSC Ensembl
Innerchr20:26126348..26246086hg19UCSC Ensembl
Outerchr20:26126348..26246086hg19UCSC Ensembl
Innerchr20:26074348..26194086hg18UCSC Ensembl
Outerchr20:26074348..26194086hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38119739
hg19119739
hg18119739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792932
Samples
Known GenesLOC284801, MIR663A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893329
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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