A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518778



Internal ID20892139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10608706..10609878hg38UCSC Ensembl
chr19:10719382..10720554hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198037
Samples
Known GenesSLC44A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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