A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052076



Internal ID102568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93552237..93552535hg38UCSC Ensembl
chr11:93285403..93285701hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052076
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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