A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226313



Internal ID22369155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56365905..56366003hg38UCSC Ensembl
chr20:54940961..54941059hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300336
SamplesNA19238
Known GenesFAM210B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226313
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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