A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525951



Internal ID22395330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120296566..120297169hg38UCSC Ensembl
chrX:119430421..119431024hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10261n152
Supporting Variantsnssv14352704, nssv14352703
SamplesNA19239, NA19240
Known GenesTMEM255A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525951
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