A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525408



Internal ID22394786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16700168..16700499hg38UCSC Ensembl
chrX:16718291..16718622hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349956, nssv14349958, nssv14349959, nssv14349957
SamplesNA19238, HG00731, HG00732, NA19240
Known GenesCTPS2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525408
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer