A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6734n152



Internal ID22822437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89097202..89097290hg38UCSC Ensembl
chr4:90018353..90018441hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3210160, nsv3195140
SamplesHG00514
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)dgv6734n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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