A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891854



Internal ID19186250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68106900..68213569hg38UCSC Ensembl
Outerchr10:68106900..68213569hg38UCSC Ensembl
Innerchr10:69866657..69973326hg19UCSC Ensembl
Outerchr10:69866657..69973326hg19UCSC Ensembl
Innerchr10:69536663..69643332hg18UCSC Ensembl
Outerchr10:69536663..69643332hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38106670
hg19106670
hg18106670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792107
Samples
Known GenesMYPN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891854
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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