A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023227



Internal ID83205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69416552..69438276hg38UCSC Ensembl
chr9:72031468..72053192hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821725
hg1921725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141699
Supporting Variants
Samples
Known GenesAPBA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023227
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.028585


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