A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027147



Internal ID21936490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68710900..68711007hg38UCSC Ensembl
chr16:68744803..68744910hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027147
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