A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581386



Internal ID21529884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159507663..159507732hg38UCSC Ensembl
chr6:159928695..159928764hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142375
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581386
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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