A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065738



Internal ID21508174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40937501..40937501hg38UCSC Ensembl
chr1:41403173..41403173hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg382889
hg192889
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616721
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065738
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