A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530706



Internal ID20904067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20966132..21001087hg38UCSC Ensembl
chr19:21148938..21183893hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3834956
hg1934956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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