A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728871



Internal ID152537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37785249..37790253hg38UCSC Ensembl
chr22:38181256..38186260hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385005
hg195005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546160
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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