A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219687



Internal ID22364634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49218242..49219013hg38UCSC Ensembl
chr20:47834779..47835550hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299441
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219687
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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