A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072899



Internal ID21501810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120516931..120517656hg38UCSC Ensembl
chr11:120387640..120388365hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590155
Supporting Variants
SamplesNA19239
Known GenesGRIK4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072899
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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