A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1634n152



Internal ID22817337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131633687..131633766hg38UCSC Ensembl
chr11:131503581..131503660hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3228627, nsv3211611
SamplesNA19239, NA19240
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)dgv1634n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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