A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624361



Internal ID21816408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26593168..26593168hg38UCSC Ensembl
chr16:26604489..26604489hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081748
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624361
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