A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024162



Internal ID83838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66773387..66986693hg38UCSC Ensembl
chr9:40706148..40919495hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38213307
hg19213348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141526
Supporting Variants
Samples
Known GenesFAM74A3, SPATA31A3, ZNF658
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024162
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01482


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