A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv971n152



Internal ID22816674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67783874..67797085hg38UCSC Ensembl
chr10:69543632..69556843hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3813212
hg1913212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3227629, nsv3223381
SamplesHG00732, HG00733
Known GenesDNAJC12
MethodOptical mapping
Sequencing
AnalysisBioNano Genomics proprietary analysis
Multiple analysis algorthms
PlatformBioNano Genomics
Illumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv971n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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