A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519260



Internal ID20892621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46507542..46510014hg38UCSC Ensembl
chr19:47010799..47013271hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382473
hg192473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046810
Samples
Known GenesPPP5D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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