A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045554



Internal ID98131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59925304..59926820hg38UCSC Ensembl
chr11:59692777..59694293hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381517
hg191517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045554
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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