A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045228



Internal ID97902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66130397..66130503hg38UCSC Ensembl
chr11:65897868..65897974hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502624
Supporting Variants
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045228
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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