A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592079



Internal ID21540659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135615200..135615264hg38UCSC Ensembl
chr9:138507046..138507110hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160542
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592079
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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