A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534945



Internal ID20908306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53641590..53651963hg38UCSC Ensembl
chr19:54144844..54155217hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3810374
hg1910374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534945
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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