A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134760



Internal ID21505559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13147547..13147547hg38UCSC Ensembl
chr4:13149171..13149171hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382470
hg192470
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618631
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134760
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