A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088609



Internal ID21997842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5551088..5551088hg38UCSC Ensembl
chr9:5551088..5551088hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579190
Samples
Known GenesPDCD1LG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088609
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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