A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663566



Internal ID21611871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42280178..42280178hg38UCSC Ensembl
chr13:42854314..42854314hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094906
SamplesHG02587
Known GenesAKAP11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663566
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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