A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1077n152



Internal ID22816780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119531909..119572986hg38UCSC Ensembl
chr10:121291421..121332498hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3841078
hg1941078
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3249163, nsv3232359
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesRGS10
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1077n152
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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