A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072772



Internal ID21470011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125457421..125457482hg38UCSC Ensembl
chr11:125327317..125327378hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586852
Supporting Variants
SamplesHG03125
Known GenesFEZ1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072772
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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