A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651561



Internal ID21599866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39706255..39706255hg38UCSC Ensembl
chr13:40280392..40280392hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094200
SamplesHG03683
Known GenesCOG6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651561
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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