A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263710



Internal ID20472928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39111621..39111704hg38UCSC Ensembl
chr20:37740264..37740347hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263710
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