A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425561



Internal ID21083114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49035201..49045500hg38UCSC Ensembl
chr8:49947760..49958059hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425561
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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