A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057672



Internal ID21966905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35925859..35926075hg38UCSC Ensembl
chr20:34513781..34513997hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624355
Samples
Known GenesPHF20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057672
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