A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7756n152



Internal ID22823459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266086..16266162hg38UCSC Ensembl
chr6:16266317..16266393hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3527510, nsv3284599
SamplesHG00512, NA19238, NA19239, NA19240, HG00514
Known GenesGMPR
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)dgv7756n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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