A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046208



Internal ID21955453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36265240..36308234hg38UCSC Ensembl
chr19:36756142..36799136hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3842995
hg1942995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046208
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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