A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211259



Internal ID22358874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88546259..88559653hg38UCSC Ensembl
Outerchr16:88612667..88626061hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3813395
hg1913395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14260292
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211259
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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