A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427105



Internal ID21084658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9629501..9677400hg38UCSC Ensembl
chr8:9487011..9534910hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3847900
hg1947900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7234n223
Supporting Variantsnssv18237049
Samples
Known GenesTNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427105
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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