A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418013



Internal ID21075566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9550501..9573300hg38UCSC Ensembl
chr8:9408011..9430810hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3822800
hg1922800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236524
Samples
Known GenesTNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418013
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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