A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226411



Internal ID22369220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19273830..19274257hg38UCSC Ensembl
chr20:19254474..19254901hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14297597, nssv14297598
SamplesNA19239, HG00514
Known GenesLOC100130264, SLC24A3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226411
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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