A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100546



Internal ID22009779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57435223..57435223hg38UCSC Ensembl
chr19:57946591..57946591hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100546
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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