A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14259885



Internal ID22256449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:71290499..71304315hg38UCSC Ensembl
Outerchr16:71324402..71338218hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg382358
hg192358
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3246192
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14259885
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