A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428157



Internal ID21085710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115359268..115379988hg38UCSC Ensembl
chr8:116371497..116392217hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3820721
hg1920721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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