A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588416



Internal ID21780459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89484759..89484895hg38UCSC Ensembl
chr9:92099674..92099810hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588416
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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