A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546890



Internal ID18747966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115952154..115952481hg38UCSC Ensembl
Outerchr10:115952021..115952564hg38UCSC Ensembl
Innerchr10:117711665..117711992hg19UCSC Ensembl
Outerchr10:117711532..117712075hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745637
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546890
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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