A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225335



Internal ID22368496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36958700..36959195hg38UCSC Ensembl
chr22:37354741..37355236hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303536, nssv14303535
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225335
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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