A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658620



Internal ID21606925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39059254..39059254hg38UCSC Ensembl
chr13:39633391..39633391hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097485
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658620
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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