A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583838



Internal ID21775881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128710004..128710102hg38UCSC Ensembl
chr9:131472283..131472381hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018650
Supporting Variants
Samples
Known GenesPKN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583838
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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