A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018266



Internal ID21927609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11533619..11573428hg38UCSC Ensembl
chr8:11391128..11430937hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3839810
hg1939810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572108
Samples
Known GenesBLK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018266
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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