A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220975



Internal ID22365511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27336134..27338400hg38UCSC Ensembl
chr18:24916098..24918364hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382267
hg192267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14290929
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220975
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