A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024233



Internal ID83895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68292552..68337700hg38UCSC Ensembl
chr9:70907468..70952616hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3845149
hg1945149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142925
Supporting Variants
Samples
Known GenesCBWD3, FOXD4L3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024233
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.486559


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