A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14255761



Internal ID22131520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:123888696..123907526hg38UCSC Ensembl
Outerchr11:123759403..123778233hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3239518
Supporting Variants
SamplesHG00513
Known GenesOR8D4
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14255761
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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