A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3532397



Internal ID22401724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46391946..46391999hg38UCSC Ensembl
chr19:46895203..46895256hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291542, nssv14291540, nssv14291541
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3532397
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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