A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238951



Internal ID22374297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1425610..1433783hg38UCSC Ensembl
Outerchr11:1446840..1455013hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254252
SamplesNA19238
Known GenesBRSK2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238951
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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