A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088960



Internal ID21998193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32977146..32977146hg38UCSC Ensembl
chr9:32977144..32977144hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589359
Samples
Known GenesAPTX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088960
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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