A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016904



Internal ID21926247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132986240..132986292hg38UCSC Ensembl
chr9:135861627..135861679hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579847
Samples
Known GenesGFI1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016904
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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