A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519473



Internal ID20892834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4169461..4214852hg38UCSC Ensembl
chr19:4169458..4214849hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3845392
hg1945392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198818
Samples
Known GenesANKRD24, CREB3L3, SIRT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519473
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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