A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219932



Internal ID22364793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30454865..30454931hg38UCSC Ensembl
chr22:30850852..30850918hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5706n152
Supporting Variantsnssv14304825, nssv14304824
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219932
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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