A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635259



Internal ID21583564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5560685..5560685hg38UCSC Ensembl
chr9:5560685..5560685hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162096
SamplesHG02818
Known GenesPDCD1LG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635259
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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