A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9574n152



Internal ID22825277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65798555..65861624hg38UCSC Ensembl
chr9:42779142..42842202hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3863070
hg1963061
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3243490, nsv3230862
SamplesHG00512, NA19238, HG00731, HG00732, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9574n152
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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