A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050642



Internal ID101642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107082824..107569791hg38UCSC Ensembl
chr11:106953550..107440517hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38486968
hg19486968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498592
Supporting Variants
Samples
Known GenesALKBH8, CWF19L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050642
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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