A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519511



Internal ID20892872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44940698..44943746hg38UCSC Ensembl
chr19:45443955..45447003hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383049
hg193049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048206
Samples
Known GenesAPOC4, APOC4-APOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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