A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528067



Internal ID20901428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44730211..44736297hg38UCSC Ensembl
chr19:45233478..45239553hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386087
hg196076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198851
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528067
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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