A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228654



Internal ID22370771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35683865..35683930hg38UCSC Ensembl
chr22:36079912..36079977hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305623
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228654
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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