A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1861n152



Internal ID22817564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57834865..57835446hg38UCSC Ensembl
chr12:58228648..58229229hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3217206, nsv3214742
SamplesNA19240
Known GenesCTDSP2
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)dgv1861n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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