A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14258149



Internal ID22279465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:49753405..49766954hg38UCSC Ensembl
Outerchr14:50220123..50233672hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg387420
hg197420
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3249810
Supporting Variants
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14258149
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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