A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352094



Internal ID22577763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43065839..43066004hg38UCSC Ensembl
chr11:43087389..43087554hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352094
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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