A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022506



Internal ID82684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40002000..40159000hg38UCSC Ensembl
chr9:42147018..42304018hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38157001
hg19157001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141772
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022506
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.096094


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