A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523840



Internal ID20897201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4320673..4321522hg38UCSC Ensembl
chr19:4320670..4321519hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198568
Samples
Known GenesFSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523840
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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