A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017316



Internal ID21926659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113673239..113674413hg38UCSC Ensembl
chr9:116435519..116436693hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381175
hg191175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017316
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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