A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097269



Internal ID22006502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14470347..14470347hg38UCSC Ensembl
chr16:14564204..14564204hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610764
Samples
Known GenesPARN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097269
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