A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1036n71



Internal ID6318656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17476516..17491386hg19UCSC Ensembl
chr11:17433092..17447962hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv897020, nsv897021
SamplesSP56914, IS38390, IS40757
Known GenesABCC8
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1036n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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