A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051397



Internal ID102121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109633756..109640546hg38UCSC Ensembl
chr11:109504482..109511272hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386791
hg196791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051397
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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