A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220726



Internal ID22365337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:158123889..158148207hg38UCSC Ensembl
Outerchr3:157841678..157865996hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg382517
hg192517
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271957
SamplesNA19238
Known GenesRSRC1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220726
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