A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3237401



Internal ID22373867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113343372..113371387hg38UCSC Ensembl
Outerchr13:113997687..114025702hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2490n152
Supporting Variantsnssv14257470
SamplesNA19238
Known GenesGRTP1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3237401
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