A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049719



Internal ID101040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86879168..86879897hg38UCSC Ensembl
chr11:86590210..86590939hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049719
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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