A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047695



Internal ID99667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69281653..69288870hg38UCSC Ensembl
chr11:69049120..69056337hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg387218
hg197218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047695
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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