A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3235709



Internal ID22373371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103330001..103349784hg38UCSC Ensembl
Outerchr10:105089758..105109541hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg386204
hg196204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253491
SamplesHG00731
Known GenesPCGF6
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3235709
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