A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1036n152



Internal ID22816739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102885480..102885830hg38UCSC Ensembl
chr10:104645237..104645587hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3522926, nsv3175280
SamplesHG00512, NA19239, HG00732, HG00733, HG00513, HG00514
Known GenesAS3MT, C10orf32-ASMT
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)dgv1036n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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