A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584967



Internal ID21533511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88194541..88198103hg38UCSC Ensembl
chr16:88228147..88231709hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383563
hg193563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096078
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584967
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer