A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033782



Internal ID21943125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88122048..88122564hg38UCSC Ensembl
chr16:88155654..88156170hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033782
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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