A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052031



Internal ID102536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93134896..93142948hg38UCSC Ensembl
chr11:92868062..92876114hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388053
hg198053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052031
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.020087


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