A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028009



Internal ID21937352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47996031..47996098hg38UCSC Ensembl
chr16:48029942..48030009hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624510
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028009
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