A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196441



Internal ID22346447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10799340..10799455hg38UCSC Ensembl
chr5:10799452..10799567hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14320208
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196441
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