A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9639n152



Internal ID22825342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86979404..87021707hg38UCSC Ensembl
chr9:89594319..89636622hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3842304
hg1942304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3247993, nsv3239965
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesLOC100506834, LOC440173
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9639n152
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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