A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049708



Internal ID101033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86827332..86832677hg38UCSC Ensembl
chr11:86538374..86543719hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg385346
hg195346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496249
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049708
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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