A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641478



Internal ID21589783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6360917..6360917hg38UCSC Ensembl
chr5:6361030..6361030hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145843
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641478
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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