A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060357



Internal ID21969590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8104519..8104888hg38UCSC Ensembl
chr19:8169403..8169772hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627359
Samples
Known GenesFBN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060357
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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