A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053438



Internal ID103474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125505373..125505872hg38UCSC Ensembl
chr11:125375269..125375768hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053438
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001717


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