A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1464n152



Internal ID22817167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73462807..73463071hg38UCSC Ensembl
chr11:73173852..73174116hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3218193, nsv3223399
SamplesHG00512, NA19240
Known GenesFAM168A
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)dgv1464n152
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