A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1639n152



Internal ID22817342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131865835..131865970hg38UCSC Ensembl
chr11:131735729..131735864hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3212844, nsv3219125
SamplesNA19238, HG00731, NA19240, HG00733, HG00513, HG00514
Known GenesNTM
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)dgv1639n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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