A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213285



Internal ID22360277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51976449..51976914hg38UCSC Ensembl
chr20:50592988..50593453hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299530, nssv14299529
SamplesNA19238, HG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213285
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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