A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14282997



Internal ID22278278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:41750038..42219216hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3843456
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3247477
Supporting Variants
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14282997
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer