A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075802



Internal ID21498209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69813576..69813647hg38UCSC Ensembl
chr11:69628344..69628415hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584748
Supporting Variants
SamplesNA19238
Known GenesFGF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075802
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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