A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045549



Internal ID98126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59834251..59834271hg38UCSC Ensembl
chr11:59601724..59601744hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538660
Supporting Variants
Samples
Known GenesGIF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045549
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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