A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090270



Internal ID21999503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69361931..69361931hg38UCSC Ensembl
chr16:69395834..69395834hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627704
Samples
Known GenesTERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090270
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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