A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519481



Internal ID20892842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10825263..10844576hg38UCSC Ensembl
chr19:10935939..10955252hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3819314
hg1919314
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198045
Samples
Known GenesDNM2, MIR6793, TMED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519481
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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