A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431465



Internal ID21089018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69781775..69808414hg38UCSC Ensembl
chr8:70694010..70720649hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3826640
hg1926640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235495
Samples
Known GenesSLCO5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431465
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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