A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1207n152



Internal ID22816910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:881582..881656hg38UCSC Ensembl
chr11:881582..881656hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3217129, nsv3228754
SamplesNA19239, NA19240
Known GenesCHID1
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)dgv1207n152
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