A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533623



Internal ID20906984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33743558..33765817hg38UCSC Ensembl
chr19:34234463..34256722hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3822260
hg1922260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197747
Samples
Known GenesCHST8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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