A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047193



Internal ID99303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75098814..75098814hg38UCSC Ensembl
chr11:74809859..74809859hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551168
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047193
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02236


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