A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034101



Internal ID21943444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50962505..50966063hg38UCSC Ensembl
chr18:48488875..48492433hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg383559
hg193559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034101
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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