A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074078



Internal ID21457772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2025770..2025770hg38UCSC Ensembl
chr11:2047000..2047000hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382481
hg192481
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654615
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074078
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