A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281557



Internal ID20490775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16538404..16538589hg38UCSC Ensembl
chr19:16649215..16649400hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733475
Supporting Variants
Samples
Known GenesCHERP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281557
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