A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516642



Internal ID20890003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46669854..46683344hg38UCSC Ensembl
chr19:47173111..47186601hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3813491
hg1913491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046822
Samples
Known GenesDACT3-AS1, PRKD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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