A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043152



Internal ID96475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5305299..5305350hg38UCSC Ensembl
chr11:5326529..5326580hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043152
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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