A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210369



Internal ID22358298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:109774019..109827746hg38UCSC Ensembl
Outerchr10:111533777..111587504hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3853728
hg1953728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278902, nssv14278895, nssv14278901, nssv14278898, nssv14278897, nssv14278899, nssv14278900, nssv14278894, nssv14278896
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210369
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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