A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105912



Internal ID22015145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46635674..46635674hg38UCSC Ensembl
chr19:47138931..47138931hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105912
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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