A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600186



Internal ID21792233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51412690..51412793hg38UCSC Ensembl
chr14:51879408..51879511hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600186
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