A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528561



Internal ID20901922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3328177..3348901hg38UCSC Ensembl
chr19:3328175..3348899hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3820725
hg1920725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528561
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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