A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562446



Internal ID22431200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44926026..44926026hg38UCSC Ensembl
chr22:45321906..45321906hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14304449, nssv14304448
SamplesHG00512, HG00732
Known GenesPHF21B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562446
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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