A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288445



Internal ID20497663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46078801..46078919hg38UCSC Ensembl
chr19:46582059..46582177hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288445
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