A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228632



Internal ID22370755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:32349446..32384013hg38UCSC Ensembl
Outerchr11:32370992..32405559hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3834568
hg1934568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254413, nssv14254414, nssv14254412
SamplesNA19240, HG00733, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228632
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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