A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1079n152



Internal ID22816782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120798368..120798510hg38UCSC Ensembl
chr10:122557880..122558022hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3287739, nsv3528145
SamplesNA19239, HG00732, NA19240
Known GenesMIR5694, WDR11-AS1
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)dgv1079n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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