A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2962n152



Internal ID22818665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67242127..67242462hg38UCSC Ensembl
chr15:67534465..67534800hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3189421, nsv3522832
SamplesHG00512, HG00731, HG00732, HG00733, HG00514
Known GenesAAGAB
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)dgv2962n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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