A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275762



Internal ID20484980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133105811..133105868hg38UCSC Ensembl
chr9:135981198..135981255hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739960
Supporting Variants
Samples
Known GenesRALGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275762
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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