A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029318



Internal ID21938661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12411322..12411400hg38UCSC Ensembl
chr18:12411321..12411399hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633097
Samples
Known GenesSLMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029318
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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