A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220697



Internal ID22365318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37487445..37488382hg38UCSC Ensembl
chr20:36115847..36116784hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300636
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220697
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer