A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226671



Internal ID22369391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:117631261..117678270hg38UCSC Ensembl
Outerchr10:119390772..119437781hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3847010
hg1947010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14280647
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226671
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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