A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215805



Internal ID22362012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61601844..61602238hg38UCSC Ensembl
chr18:59269077..59269471hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285514, nssv14285515
SamplesHG00512, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215805
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