A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586333



Internal ID21534886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135518594..135518644hg38UCSC Ensembl
chr9:138410440..138410490hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161068
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586333
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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