A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571111



Internal ID21519484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:909370..910309hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140629
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571111
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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