A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029422



Internal ID21938765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12368600..12368651hg38UCSC Ensembl
chr18:12368599..12368650hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625797
Samples
Known GenesAFG3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029422
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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