A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14275226



Internal ID22299730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:74216862..74228331hg38UCSC Ensembl
Outerchr5:73512687..73524156hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg383810
hg193810
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222068
Supporting Variants
SamplesNA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14275226
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