A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6869n152



Internal ID22822572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141709003..141709055hg38UCSC Ensembl
chr4:142630156..142630208hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3209881, nsv3200335
SamplesHG00512, HG00733, HG00514
Known GenesIL15
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)dgv6869n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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