A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274144



Internal ID20483362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114486907..114486969hg38UCSC Ensembl
chr9:117249187..117249249hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749170
Supporting Variants
Samples
Known GenesDFNB31
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274144
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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