A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027883



Internal ID21937226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:64715076..64966563hg38UCSC Ensembl
chr18:62382311..62633799hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38251488
hg19251489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027883
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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