A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049432



Internal ID100845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100923471..100925560hg38UCSC Ensembl
chr11:100794202..100796291hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382090
hg192090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505402
Supporting Variants
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049432
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003435


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