A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024699



Internal ID84199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36837764..36837860hg38UCSC Ensembl
chr9:36837761..36837857hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489780
Supporting Variants
Samples
Known GenesPAX5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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