A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042796



Internal ID96236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38404392..38404430hg38UCSC Ensembl
chr11:38425942..38425980hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552734
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042796
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001873


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