A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354796



Internal ID22580465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10929623..10929623hg38UCSC Ensembl
chr11:10951170..10951170hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968686
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354796
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer