A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019490



Internal ID21928833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1141779..1142250hg38UCSC Ensembl
chr6:1142014..1142485hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019490
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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