A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021002



Internal ID81640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5560702..5560753hg38UCSC Ensembl
chr9:5560702..5560753hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5396072
Supporting Variants
Samples
Known GenesPDCD1LG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021002
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.016235


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