A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547059



Internal ID18748135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129796961..129797207hg38UCSC Ensembl
Outerchr10:129796901..129797237hg38UCSC Ensembl
Innerchr10:131595225..131595471hg19UCSC Ensembl
Outerchr10:131595165..131595501hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745806
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547059
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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