A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453659



Internal ID21111212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71960851..71961435hg38UCSC Ensembl
chr9:74575767..74576351hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219295
Samples
Known GenesC9orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453659
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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