A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146371



Internal ID345576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50054874..50091150hg38UCSC Ensembl
chr19:50558131..50594407hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3836277
hg1936277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724065
Samples
Known GenesFLJ26850
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146371
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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