A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546872



Internal ID18747948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113448060..113457032hg38UCSC Ensembl
Outerchr10:113447140..113457299hg38UCSC Ensembl
Innerchr10:115207819..115216791hg19UCSC Ensembl
Outerchr10:115206899..115217058hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3810160
hg1910160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745619
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546872
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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