A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580083



Internal ID21528569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21551378..21551734hg38UCSC Ensembl
chr6:21551609..21551965hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156747
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580083
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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