A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14271576



Internal ID22266934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:147872433..147900836hg38UCSC Ensembl
Outerchr3:147590220..147618623hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382257
hg192257
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218790
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14271576
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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