A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072514



Internal ID21482505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114394174..114394174hg38UCSC Ensembl
chr11:114264896..114264896hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652858
Supporting Variants
SamplesHG03732
Known GenesC11orf71
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072514
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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