A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021320



Internal ID81849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30522161..30646696hg38UCSC Ensembl
chr9:30522159..30646694hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38124536
hg19124536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021320
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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