A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020235



Internal ID21929578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114459139..114459212hg38UCSC Ensembl
chr9:117221419..117221492hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594204
Samples
Known GenesDFNB31
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020235
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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