A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614428



Internal ID21806475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22765212..22766279hg38UCSC Ensembl
chr14:23234421..23235488hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032981
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614428
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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