A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427850



Internal ID21085403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48122591..48129180hg38UCSC Ensembl
chr8:49035151..49041740hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg386590
hg196590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427850
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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