A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145819



Internal ID345024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36426489..36498923hg38UCSC Ensembl
chr19:36917391..36989825hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3872435
hg1972435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723096
Samples
Known GenesLOC728752, ZNF566
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145819
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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