A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745299



Internal ID18719545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79965538..79967670hg38UCSC Ensembl
Outerchr10:79965253..79967684hg38UCSC Ensembl
Innerchr10:81725294..81727426hg19UCSC Ensembl
Outerchr10:81725009..81727440hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382432
hg192432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546552
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745299
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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