A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033166



Internal ID21942509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23762379..23766399hg38UCSC Ensembl
chr16:23773700..23777720hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384021
hg194021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033166
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