A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045511



Internal ID98100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59477074..59492000hg38UCSC Ensembl
chr11:59244547..59259473hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3814927
hg1914927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501379
Supporting Variants
Samples
Known GenesOR4D10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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