A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659591



Internal ID21607896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4613885..4613885hg38UCSC Ensembl
chr16:4663886..4663886hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385501
hg195501
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089673
SamplesHG03009
Known GenesUBALD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659591
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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