A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044262



Internal ID97248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35986025..35986025hg38UCSC Ensembl
chr11:36007575..36007575hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5411051
Supporting Variants
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044262
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.038546


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