A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534758



Internal ID20908119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47605313..47606075hg38UCSC Ensembl
chr19:48108570..48109332hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534758
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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