A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042138



Internal ID95800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3084757..3085779hg38UCSC Ensembl
chr11:3105987..3107009hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042138
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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