A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059091



Internal ID21968324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52289280..52289416hg38UCSC Ensembl
chr19:52792533..52792669hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625941
Samples
Known GenesZNF766
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059091
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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