A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075803



Internal ID21468466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69813600..69813600hg38UCSC Ensembl
chr11:69628368..69628368hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658107
Supporting Variants
SamplesHG03125
Known GenesFGF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075803
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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