A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353398



Internal ID22579067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94508192..94514054hg38UCSC Ensembl
chr11:94241358..94247220hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385863
hg195863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921405
Supporting Variants
Samples
Known GenesLOC643037
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353398
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