A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024943



Internal ID84354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65282000..65296082hg38UCSC Ensembl
chr9:70175606..70189688hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3814083
hg1914083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142618
Supporting Variants
Samples
Known GenesFOXD4L5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024943
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.072686


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