A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064760



Internal ID21442788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32986772..32986772hg38UCSC Ensembl
chr1:33452373..33452373hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381587
hg191587
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606225
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064760
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