A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492789



Internal ID269991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71960851..71961341hg38UCSC Ensembl
chr9:74575767..74576257hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024284
Samples
Known GenesC9orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492789
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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