A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043304



Internal ID96580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10888373..10888424hg38UCSC Ensembl
chr11:10909920..10909971hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5396751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043304
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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