A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049125



Internal ID100634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108385232..108396179hg38UCSC Ensembl
chr11:108255959..108266906hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810948
hg1910948
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143526
Supporting Variants
Samples
Known GenesC11orf65
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049125
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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