A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046191



Internal ID98592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66448471..66453535hg38UCSC Ensembl
chr11:66215942..66221006hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385065
hg195065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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