A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587763



Internal ID21779806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59903433..59903511hg38UCSC Ensembl
chr11:59670906..59670984hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587763
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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