A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654374



Internal ID21602679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85984238..85984238hg38UCSC Ensembl
chr16:86017844..86017844hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381387
hg191387
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081272
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654374
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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