A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043961



Internal ID97039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42421520..42495049hg38UCSC Ensembl
chr11:42443070..42516599hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3873530
hg1973530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043961
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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