A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211631



Internal ID22359124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:39032681..39222616hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38189936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv886n152
Supporting Variantsnssv14278237, nssv14278727
SamplesNA19239, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211631
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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