A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14291501



Internal ID22256473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45171819..45173393hg38UCSC Ensembl
chr19:45675077..45676651hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217777
Supporting Variants
SamplesNA19238
Known GenesTRAPPC6A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14291501
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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