A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109507



Internal ID22018740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45414778..45414778hg38UCSC Ensembl
chr18:42994743..42994743hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636912
Samples
Known GenesSLC14A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109507
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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