A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2722n152



Internal ID22818425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92929294..92929375hg38UCSC Ensembl
chr14:93395639..93395720hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3529498, nsv3283469
SamplesHG00731, HG00733
Known GenesCHGA
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)dgv2722n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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