A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422343



Internal ID21079896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97486567..97639156hg38UCSC Ensembl
chr8:98498795..98651384hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38152590
hg19152590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422343
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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