A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663479



Internal ID21611784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:412047..412047hg38UCSC Ensembl
chr11:412047..412047hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074612
SamplesHG00512
Known GenesSIGIRR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663479
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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