A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043190



Internal ID96500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5678676..5682087hg38UCSC Ensembl
chr11:5699906..5703317hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383412
hg193412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498480
Supporting Variants
Samples
Known GenesTRIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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