A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987152



Internal ID20554194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117405746..117407583hg38UCSC Ensembl
chr11:117276462..117278299hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381838
hg191838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468740
Supporting Variants
Samples
Known GenesCEP164
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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