A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14285708



Internal ID22271361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:82825..129048hg38UCSC Ensembl
chr19:82825..129048hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3846224
hg1946224
Variant TypeCNV duplication
Copy Number8
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225972
Supporting Variants
SamplesNA19239
Known GenesOR4F17
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14285708
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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