A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520963



Internal ID20894324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12632672..12634150hg38UCSC Ensembl
chr19:12743486..12744964hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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