A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043683



Internal ID96849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18209136..18209183hg38UCSC Ensembl
chr11:18230683..18230730hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545173
Supporting Variants
Samples
Known GenesLOC494141
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043683
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.022635


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