A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001978



Internal ID21911321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94750346..94750464hg38UCSC Ensembl
chr9:97512628..97512746hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589939
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001978
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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