A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252760



Internal ID22266857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:102635341..102647171hg38UCSC Ensembl
Outerchr10:104395098..104406928hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3241964
Supporting Variants
SamplesNA19238
Known GenesTRIM8
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14252760
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