A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214338



Internal ID22361019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36461001..36461657hg38UCSC Ensembl
chr22:36857048..36857704hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305643, nssv14305644
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214338
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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