A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043759



Internal ID96904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38831939..38940355hg38UCSC Ensembl
chr11:38853489..38961905hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38108417
hg19108417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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