A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146437



Internal ID345642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55454874..55460874hg38UCSC Ensembl
chr19:55966241..55972241hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725678
Samples
Known GenesISOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146437
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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