A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225972



Internal ID22368941
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285704, nssv14285703, nssv14285705, nssv14285707, nssv14285708, nssv14285701, nssv14285709, nssv14285706, nssv14285702
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesOR4F17
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225972
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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