A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262615



Internal ID20471833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62816643..62817051hg38UCSC Ensembl
chr14:63283361..63283769hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742219
Supporting Variants
Samples
Known GenesKCNH5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262615
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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