A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728914



Internal ID152580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38291227..38291403hg38UCSC Ensembl
chr22:38687233..38687409hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535826
Supporting Variants
Samples
Known GenesCSNK1E
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728914
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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