A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211635



Internal ID22359128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:32016115..32027762hg38UCSC Ensembl
Outerchr14:32485321..32496968hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3811648
hg1911648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258895
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211635
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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