A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212163



Internal ID22359497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26270670..26270756hg38UCSC Ensembl
chr18:23850634..23850720hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14290899, nssv14290900
SamplesNA19239, NA19240
Known GenesTAF4B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212163
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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