A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9624n152



Internal ID22825327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82510397..82510486hg38UCSC Ensembl
chr9:85125312..85125401hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3288255, nsv3288236, nsv3285087, nsv3220719
SamplesHG00512, NA19238, NA19240, HG00733, 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)dgv9624n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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