A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216282



Internal ID22362321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:57447301..57507696hg38UCSC Ensembl
Outerchr10:59207061..59267456hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3860396
hg1960396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278822, nssv14278821
SamplesNA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216282
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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