A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612652



Internal ID21804699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25246521..25398214hg38UCSC Ensembl
chr14:25715727..25867420hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38151694
hg19151694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612652
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