A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290808



Internal ID20500026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73672310..73672539hg38UCSC Ensembl
chr14:74139013..74139242hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750270
Supporting Variants
Samples
Known GenesDNAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290808
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