A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112360



Internal ID22021593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4641499..4641499hg38UCSC Ensembl
chr18:4641499..4641499hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112360
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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