A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075307



Internal ID21486802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67118461..67118461hg38UCSC Ensembl
chr11:66885932..66885932hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644697
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075307
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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