A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425259



Internal ID21082812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23484794..23495234hg38UCSC Ensembl
chr8:23342307..23352747hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3810441
hg1910441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425259
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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