A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706543



Internal ID21378819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39708988..39709124hg38UCSC Ensembl
chr20:38337630..38337766hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392556
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706543
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.554598


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer