A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616716



Internal ID21565021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138134067..138134067hg38UCSC Ensembl
chr4:139055221..139055221hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123781
SamplesNA20509
Known GenesSLC7A11-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616716
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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