A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211537



Internal ID22359065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:44232866..44267716hg38UCSC Ensembl
Outerchr22:44628746..44663596hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3834851
hg1934851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14269376
SamplesHG00513
Known GenesKIAA1644
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211537
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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