A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14253456



Internal ID22144328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131819207..131888064hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385027
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3234298
Supporting Variants
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14253456
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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