A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585732



Internal ID21777775
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 StatusS
Merged Variantsnsv6017316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585732
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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