A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375792



Internal ID22327366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101917751..101919350hg38UCSC Ensembl
chr14:102384088..102385687hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218122
Supporting Variants
SamplesNA19240
Known GenesPPP2R5C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375792
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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