A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047959



Internal ID99837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63519639..63520883hg38UCSC Ensembl
chr11:63287111..63288355hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499340
Supporting Variants
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047959
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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