A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728925



Internal ID152591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38430284..38431988hg38UCSC Ensembl
chr22:38826289..38827993hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535152
Supporting Variants
Samples
Known GenesKCNJ4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728925
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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