A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726824



Internal ID150490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38252521..38252678hg38UCSC Ensembl
chr21:39624443..39624600hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550417
Supporting Variants
Samples
Known GenesKCNJ15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726824
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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