A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv926n152



Internal ID22816629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49335402..49335653hg38UCSC Ensembl
chr10:50543447..50543698hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3286137, nsv3528764
SamplesHG00512, NA19238, NA19240, HG00513, HG00514
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)dgv926n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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