A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205121



Internal ID22353867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20746202..20747179hg38UCSC Ensembl
chrX:20764320..20765297hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350006
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205121
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