A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14270922



Internal ID22257569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:3178619..3196238hg38UCSC Ensembl
Outerchr3:3220303..3237922hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg381399
hg191399
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223095
Supporting Variants
SamplesNA19238
Known GenesCRBN
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14270922
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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