A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891765



Internal ID18839475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16809409..16977014hg38UCSC Ensembl
Outerchr10:16809409..16977014hg38UCSC Ensembl
Innerchr10:16851408..17019013hg19UCSC Ensembl
Outerchr10:16851408..17019013hg19UCSC Ensembl
Innerchr10:16891414..17059019hg18UCSC Ensembl
Outerchr10:16891414..17059019hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38167606
hg19167606
hg18167606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792662
Samples
Known GenesCUBN, RSU1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891765
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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