A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053456



Internal ID103485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125693909..125693966hg38UCSC Ensembl
chr11:125563804..125563861hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053456
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002185


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