A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054897



Internal ID21964130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5434840..5437184hg38UCSC Ensembl
chr20:5415486..5417830hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg382345
hg192345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622761
Samples
Known GenesLINC00658
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054897
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