A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209060



Internal ID22357192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183951152..183951502hg38UCSC Ensembl
chr4:184872305..184872655hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316808, nssv14316807
SamplesHG00512, HG00732
Known GenesSTOX2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209060
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