A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220260



Internal ID22365011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5851434..5863113hg38UCSC Ensembl
Outerchr10:5893397..5905076hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3811680
hg1911680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14276448, nssv14276450, nssv14276449
SamplesNA19238, NA19239, NA19240
Known GenesANKRD16
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220260
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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