A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7703n152



Internal ID22823406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:909593..910671hg38UCSC Ensembl
chr6:910021..910943hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381079
hg19923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3199301, nsv3525413
SamplesHG00512, NA19239, NA19240, HG00513, HG00514
Known Genes
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)dgv7703n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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