A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093045



Internal ID21279575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44250906..44252677hg38UCSC Ensembl
Innerchr11:44272456..44274227hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381772
hg191772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110599
Supporting Variants
Samplessample286
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093045
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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