A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595635



Internal ID21787678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113307293..113308159hg38UCSC Ensembl
chr9:116069573..116070439hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595635
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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