A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9611n152



Internal ID22825314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79987000..79987058hg38UCSC Ensembl
chr9:82601915..82601973hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3213434, nsv3225157
SamplesNA19238, NA19240
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)dgv9611n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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