A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528837



Internal ID20902198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:285605..286248hg38UCSC Ensembl
chr19:285605..286248hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199369
Samples
Known GenesPPAP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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