A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222909



Internal ID22366835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55083905..55084214hg38UCSC Ensembl
chr20:53700444..53700753hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300252
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222909
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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