A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046114



Internal ID98536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44254026..44254105hg38UCSC Ensembl
chr11:44275576..44275655hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046114
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003751


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