A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646369



Internal ID21594674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26724005..26724005hg38UCSC Ensembl
chr13:27298142..27298142hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092279
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646369
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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