A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729157



Internal ID152823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41631294..41631408hg38UCSC Ensembl
chr22:42027298..42027412hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550845
Supporting Variants
Samples
Known GenesXRCC6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729157
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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