A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043380



Internal ID96636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24266033..24266246hg38UCSC Ensembl
chr11:24287579..24287792hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143847
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043380
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.064976


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