A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286151



Internal ID22200588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14852091..14903313hg38UCSC Ensembl
chr19:14962903..15014125hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3851223
hg1951223
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225446
Supporting Variants
SamplesHG00732
Known GenesOR7A17
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286151
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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