A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212405



Internal ID22359663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31515036..31517500hg38UCSC Ensembl
chr22:31911022..31913486hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg382465
hg192465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14304846
SamplesNA19239
Known GenesSFI1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212405
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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