A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224289



Internal ID22367767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46577012..46577114hg38UCSC Ensembl
chr20:45205651..45205753hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5285n152
Supporting Variantsnssv14299385
SamplesHG00733
Known GenesSLC13A3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224289
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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