A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044084



Internal ID97126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33394620..33542237hg38UCSC Ensembl
chr11:33416166..33563783hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38147618
hg19147618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044084
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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