A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1001n152



Internal ID22816704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83875042..83885037hg38UCSC Ensembl
chr10:85634798..85644793hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg389996
hg199996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3219170, nsv3216311
SamplesHG00512, HG00514
Known Genes
MethodOptical mapping
Sequencing
AnalysisBioNano Genomics proprietary analysis
Multiple analysis algorthms
PlatformBioNano Genomics
Illumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1001n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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