A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052521



Internal ID102865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114249478..114249762hg38UCSC Ensembl
chr11:114120200..114120484hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509891
Supporting Variants
Samples
Known GenesZBTB16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052521
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009681


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