A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659873



Internal ID21608178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67980874..67980874hg38UCSC Ensembl
chr16:68014777..68014777hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093425
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659873
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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