A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601980



Internal ID21550634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59392910..59393019hg38UCSC Ensembl
chr16:59426814..59426923hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087587
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601980
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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