A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746762



Internal ID18721008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75574428..75576501hg38UCSC Ensembl
Outerchr11:75574397..75576819hg38UCSC Ensembl
Innerchr11:75285473..75287546hg19UCSC Ensembl
Outerchr11:75285442..75287864hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg382423
hg192423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3548015
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746762
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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