A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098146



Internal ID22007379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30482958..30482958hg38UCSC Ensembl
chr14:30952164..30952164hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg386157
hg196157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098146
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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