A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528550



Internal ID20901911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46379095..46379797hg38UCSC Ensembl
chr19:46882352..46883054hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046794
Samples
Known GenesPPP5C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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