A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072515



Internal ID21473214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114394178..114394228hg38UCSC Ensembl
chr11:114264900..114264950hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588704
Supporting Variants
SamplesHG03371
Known GenesC11orf71
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072515
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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