A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728906



Internal ID152572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38166969..38166969hg38UCSC Ensembl
chr22:38562976..38562976hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536369
Supporting Variants
Samples
Known GenesPLA2G6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728906
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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