A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218397



Internal ID22363750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34433861..34434381hg38UCSC Ensembl
chr19:34924766..34925286hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286368
SamplesNA19239
Known GenesUBA2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218397
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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