A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048699



Internal ID100344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79599216..79599267hg38UCSC Ensembl
chr11:79310260..79310311hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408128
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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