A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049688



Internal ID101019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86643993..86644143hg38UCSC Ensembl
chr11:86355035..86355185hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501471
Supporting Variants
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049688
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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