A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636383



Internal ID21828430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12333055..12333122hg38UCSC Ensembl
chr18:12333054..12333121hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024086
Supporting Variants
Samples
Known GenesAFG3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636383
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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