A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111482



Internal ID22020716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39511299..39511299hg38UCSC Ensembl
chr19:40001939..40001939hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631349
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111482
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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