A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021300



Internal ID81838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29018540..29018612hg38UCSC Ensembl
chr9:29018538..29018610hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491817
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021300
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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