A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228557



Internal ID22370712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:16021340..16095759hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3874420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14269348, nssv14269349
SamplesHG00512, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228557
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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