A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388060



Internal ID22210760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101849672..101849672hg38UCSC Ensembl
chr14:102316009..102316009hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560393
Supporting Variants
SamplesHG00732
Known GenesPPP2R5C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388060
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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