A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532263



Internal ID20905624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56401401..56404800hg38UCSC Ensembl
chr19:56912770..56916169hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199677
Samples
Known GenesZNF583
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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