A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049149



Internal ID100652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108678783..108678819hg38UCSC Ensembl
chr11:108549510..108549546hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536278
Supporting Variants
Samples
Known GenesDDX10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049149
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.013425


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