A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209373



Internal ID22357463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226053300..226053706hg38UCSC Ensembl
chr1:226241001..226241407hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310906, nssv14310907
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209373
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