A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9747011



Internal ID18721257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102880659..102882035hg38UCSC Ensembl
Outerchr11:102880337..102882137hg38UCSC Ensembl
Innerchr11:102751389..102752765hg19UCSC Ensembl
Outerchr11:102751067..102752867hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3548264
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9747011
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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