A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220701



Internal ID22365321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50337600..50337663hg38UCSC Ensembl
chr22:50776029..50776092hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5818n152
Supporting Variantsnssv14304289, nssv14304906
SamplesNA19239, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220701
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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