A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043352



Internal ID96614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23943347..23958070hg38UCSC Ensembl
chr11:23964893..23979616hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3814724
hg1914724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499783
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043352
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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