A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045552



Internal ID98129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59903436..59903511hg38UCSC Ensembl
chr11:59670909..59670984hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045552
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003435


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