A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045540



Internal ID98118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59732943..59734424hg38UCSC Ensembl
chr11:59500416..59501897hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381482
hg191482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045540
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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