A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049138



Internal ID100644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108469074..108470675hg38UCSC Ensembl
chr11:108339801..108341402hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049138
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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