A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729152



Internal ID152818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41566048..41566683hg38UCSC Ensembl
chr22:41962052..41962687hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534748
Supporting Variants
Samples
Known GenesCSDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729152
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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