A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021526



Internal ID81997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34998000..35024000hg38UCSC Ensembl
chr9:34997997..35023997hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3826001
hg1926001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492624
Supporting Variants
Samples
Known GenesDNAJB5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021526
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000313


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