A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14274065



Internal ID22132681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:57254055..57276261hg38UCSC Ensembl
Outerchr4:58120221..58142427hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381292
hg191292
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220411
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14274065
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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