A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425792



Internal ID21083345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103529185..103540483hg38UCSC Ensembl
chr8:104541413..104552711hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3811299
hg1911299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221532
Samples
Known GenesRIMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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