A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658578



Internal ID21606883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59645321..59645321hg38UCSC Ensembl
chr11:59412794..59412794hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075550
SamplesHG00731
Known GenesPATL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658578
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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