A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020478



Internal ID21929821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31209619..31218743hg38UCSC Ensembl
chr18:28789582..28798706hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg389125
hg199125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633351
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020478
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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