A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279832



Internal ID20489050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128396145..128396325hg38UCSC Ensembl
chr9:131158424..131158604hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279832
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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