A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590451



Internal ID21539019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24509305..24509356hg38UCSC Ensembl
chr16:24520626..24520677hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083385
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590451
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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