A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058237



Internal ID21967471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43643681..43643783hg38UCSC Ensembl
chr19:44147833..44147935hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058237
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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