A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016941



Internal ID21926284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43596470..43975057hg38UCSC Ensembl
chr8:43451613..43830200hg19UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38378588
hg19378588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016941
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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