A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221932



Internal ID22366160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37227353..37227406hg38UCSC Ensembl
chr22:37623393..37623446hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5729n152
Supporting Variantsnssv14303539, nssv14303538
SamplesHG00731, HG00733
Known GenesRAC2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221932
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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