A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561379



Internal ID22429611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35116779..35116779hg38UCSC Ensembl
chr19:35607683..35607683hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286392, nssv14286393, nssv14286390, nssv14286394, nssv14286397, nssv14286395, nssv14286391, nssv14286396
SamplesHG00512, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesFXYD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561379
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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