A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358082



Internal ID22583751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119384128..119385454hg38UCSC Ensembl
chr11:119254838..119256164hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381327
hg191327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918754
Supporting Variants
Samples
Known GenesUSP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358082
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