A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050191



Internal ID101365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111158155..111162632hg38UCSC Ensembl
chr11:111028879..111033356hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384478
hg194478
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562775
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050191
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001561


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