A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526951



Internal ID20900312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54882568..54916351hg38UCSC Ensembl
chr19:55393979..55427719hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3833784
hg1933741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199602
Samples
Known GenesFCAR, NCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526951
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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