A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221854



Internal ID22366103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27325111..27325227hg38UCSC Ensembl
chr22:27721072..27721188hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5702n152
Supporting Variantsnssv14304739, nssv14304738, nssv14304740, nssv14304741
SamplesHG00512, HG00731, HG00733, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221854
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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