A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059667



Internal ID21968900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16630397..16631350hg38UCSC Ensembl
chr19:16741208..16742161hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059667
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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