A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746612



Internal ID18720858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60804006..60804424hg38UCSC Ensembl
Outerchr11:60803938..60804571hg38UCSC Ensembl
Innerchr11:60571479..60571897hg19UCSC Ensembl
Outerchr11:60571411..60572044hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746612
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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