A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023440



Internal ID21932783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47580457..47580736hg38UCSC Ensembl
chr16:47614368..47614647hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621008
Samples
Known GenesPHKB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023440
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