A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056684



Internal ID21965917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51286142..51286353hg38UCSC Ensembl
chr19:51789396..51789607hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056684
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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