A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591025



Internal ID21539597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79617680..79617744hg38UCSC Ensembl
chr16:79651577..79651641hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083430
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591025
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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