A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450746



Internal ID21108299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94707836..94732507hg38UCSC Ensembl
chr9:97470118..97494789hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3824672
hg1924672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220587
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450746
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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