A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431586



Internal ID21089139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102557401..102560100hg38UCSC Ensembl
chr8:103569629..103572328hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232415
Samples
Known GenesODF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431586
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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