A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001165



Internal ID21910508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88730..496642hg38UCSC Ensembl
chr9:88730..496642hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38407913
hg19407913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582195
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4, KANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001165
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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