A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14253396



Internal ID22116916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11235386..11249200hg38UCSC Ensembl
Outerchr11:11256933..11270747hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384259
hg194259
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3235048
Supporting Variants
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14253396
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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