A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040928



Internal ID21950266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11690213..11732184hg38UCSC Ensembl
chr19:11801028..11842999hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3841972
hg1941972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630021
Samples
Known GenesZNF823
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040928
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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