A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112635



Internal ID21295901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83544634..83546970hg38UCSC Ensembl
Innerchr11:83255677..83258013hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382337
hg192337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093256
Samplessample373
Known GenesDLG2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112635
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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