A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050177



Internal ID101355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110954997..110955054hg38UCSC Ensembl
chr11:110825721..110825778hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050177
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.027464


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