A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843309



Internal ID22026952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118305556..118305556hg38UCSC Ensembl
chr11:118176271..118176271hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258391
Supporting Variants
Samples
Known GenesCD3E
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843309
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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