A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218228



Internal ID22363637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124373516..124386561hg38UCSC Ensembl
Outerchr10:126062085..126075130hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3813046
hg1913046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277830, nssv14277831
SamplesNA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218228
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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