A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454052



Internal ID22511928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98454011..98457160hg38UCSC Ensembl
chr11:98324740..98327889hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454052
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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