A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052359



Internal ID102754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110118403..110118454hg38UCSC Ensembl
chr11:109989128..109989179hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559227
Supporting Variants
Samples
Known GenesZC3H12C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052359
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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