A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286233



Internal ID22255691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16665444..16665872hg38UCSC Ensembl
chr19:16776255..16776683hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212512
Supporting Variants
SamplesNA19238
Known GenesTMEM38A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286233
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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