A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633458



Internal ID21581763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8484617..8484617hg38UCSC Ensembl
chr9:8484617..8484617hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163080
SamplesHG03125
Known GenesPTPRD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633458
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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