A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226513



Internal ID22369289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35458422..35458505hg38UCSC Ensembl
chr19:35949324..35949407hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286402, nssv14286403, nssv14286404
SamplesNA19238, NA19240, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226513
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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