A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229332



Internal ID22371215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18937309..18937673hg38UCSC Ensembl
chr19:19048118..19048482hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14287263
SamplesHG00731
Known GenesHOMER3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229332
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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