A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051020



Internal ID101888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91761839..91808772hg38UCSC Ensembl
chr11:91495005..91541938hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3846934
hg1946934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051020
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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