A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219170



Internal ID22364278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:83875042..83885037hg38UCSC Ensembl
Outerchr10:85634798..85644793hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg389996
hg199996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1001n152
Supporting Variantsnssv14280279, nssv14280280
SamplesHG00512, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219170
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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