A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060019



Internal ID21969253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3530123..3530192hg38UCSC Ensembl
chr19:3530121..3530190hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637393
Samples
Known GenesFZR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060019
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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