A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518962



Internal ID20892323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52158462..52201526hg38UCSC Ensembl
chr19:52661715..52704779hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3843065
hg1943065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198326
Samples
Known GenesPPP2R1A, ZNF836
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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