A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986189



Internal ID20553230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105613601..105614600hg38UCSC Ensembl
chr11:105484328..105485327hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457858
Supporting Variants
Samples
Known GenesGRIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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