A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532151



Internal ID20905512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14241555..14262281hg38UCSC Ensembl
chr19:14352367..14373093hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3820727
hg1920727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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