A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213156



Internal ID22360187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:120061707..120080012hg38UCSC Ensembl
Outerchr10:121821219..121839524hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3818306
hg1918306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278843
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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