A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046144



Internal ID98559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44896085..44896994hg38UCSC Ensembl
chr11:44917636..44918545hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498225
Supporting Variants
Samples
Known GenesTSPAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046144
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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