A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657778



Internal ID21606083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112215111..112215111hg38UCSC Ensembl
chr13:112869425..112869425hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085767
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657778
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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