A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10063n152



Internal ID22825766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27527977..27528042hg38UCSC Ensembl
chrX:27546094..27546159hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3525948, nsv3281247
SamplesHG00512, NA19238, HG00732, HG00733
Known Genes
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10063n152
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