A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2853n152



Internal ID22818556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25726364..25767596hg38UCSC Ensembl
chr15:25971511..26012743hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3841233
hg1941233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3239450, nsv3235846
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesATP10A
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2853n152
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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