A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035467



Internal ID21944810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24502853..24502990hg38UCSC Ensembl
chr18:22082817..22082954hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035467
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