A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14290900



Internal ID22303735
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212163
Supporting Variants
SamplesNA19240
Known GenesTAF4B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14290900
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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