A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592279



Internal ID21784322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5516627..5516781hg38UCSC Ensembl
chr9:5516627..5516781hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003202
Supporting Variants
Samples
Known GenesPDCD1LG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592279
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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