A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468450



Internal ID22526339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115643539..115647138hg38UCSC Ensembl
chr11:115514257..115517856hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468450
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