A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435418



Internal ID21092971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62041627..62114028hg38UCSC Ensembl
chr8:62954186..63026587hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3872402
hg1972402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435418
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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