A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211492



Internal ID22359037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55696476..55698264hg38UCSC Ensembl
chr18:53363707..53365495hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381789
hg191789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14284597
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211492
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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