A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155467



Internal ID21494468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34298468..34298468hg38UCSC Ensembl
chr6:34266245..34266245hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625771
Supporting Variants
SamplesNA19238
Known GenesNUDT3, RPS10-NUDT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155467
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer