A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225407



Internal ID22368544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47954574..47954930hg38UCSC Ensembl
chr22:48350323..48350679hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303326
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225407
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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