A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046408



Internal ID98741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70164000..70164051hg38UCSC Ensembl
chr11:70010106..70010157hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5397842
Supporting Variants
Samples
Known GenesANO1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046408
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00921


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