A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744537



Internal ID18718783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3678686..3678863hg38UCSC Ensembl
Outerchr10:3678665..3678874hg38UCSC Ensembl
Innerchr10:3720878..3721055hg19UCSC Ensembl
Outerchr10:3720857..3721066hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545790
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744537
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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