A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041865



Internal ID95608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8487986..8488030hg38UCSC Ensembl
chr11:8509533..8509577hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549609
Supporting Variants
Samples
Known GenesSTK33
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041865
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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