A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026342



Internal ID21935685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:667482..667552hg38UCSC Ensembl
chr18:667482..667552hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628049
Samples
Known GenesTYMS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026342
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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