A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594204



Internal ID21786247
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 StatusS
Merged Variantsnsv6020235
Supporting Variants
Samples
Known GenesDFNB31
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594204
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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