A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14254585



Internal ID22220364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132123901..132128694hg38UCSC Ensembl
Outerchr11:131993795..131998588hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381292
hg191292
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3249798
Supporting Variants
SamplesHG00733
Known GenesNTM
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14254585
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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