A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578680



Internal ID21527152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166481711..166482042hg38UCSC Ensembl
chr6:166895199..166895530hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148347
SamplesNA19238
Known GenesRPS6KA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578680
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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