A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198421



Internal ID22348145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11717222..11717813hg38UCSC Ensembl
chrX:11735342..11735933hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10033n152
Supporting Variantsnssv14349871
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198421
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