A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525181



Internal ID20898542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58486241..58489849hg38UCSC Ensembl
chr19:58997608..59001216hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383609
hg193609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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