A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226237



Internal ID22369106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32585936..32585992hg38UCSC Ensembl
chr22:32981922..32981978hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5713n152
Supporting Variantsnssv14304884, nssv14304885
SamplesHG00732, HG00733
Known GenesSYN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226237
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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