A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432359



Internal ID21089912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15441140..15812860hg38UCSC Ensembl
chr8:15298649..15670369hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38371721
hg19371721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236370
Samples
Known GenesTUSC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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