A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053696



Internal ID103638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124443012..124443077hg38UCSC Ensembl
chr11:124312908..124312973hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511339
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053696
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.609151


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