A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649784



Internal ID21598089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27214096..27214096hg38UCSC Ensembl
chr13:27788233..27788233hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088680
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649784
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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