A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986207



Internal ID20553248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105757182..105757597hg38UCSC Ensembl
chr11:105627908..105628323hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460655
Supporting Variants
Samples
Known GenesGRIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00157


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