A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728835



Internal ID152501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37461552..37461552hg38UCSC Ensembl
chr22:37857590..37857590hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728835
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.040498


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