A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021880



Internal ID21931223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50946526..50950162hg38UCSC Ensembl
chr18:48472896..48476532hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg383637
hg193637
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621641
Samples
Known GenesME2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021880
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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