A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093867



Internal ID21507975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:34198195..34198195hg38UCSC Ensembl
chr12:34351130..34351130hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648266
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093867
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