A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422131



Internal ID21079684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93895424..93906728hg38UCSC Ensembl
chr8:94907652..94918956hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3811305
hg1911305
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422131
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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