A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567871



Internal ID21516212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152972827..152972911hg38UCSC Ensembl
chr6:153293962..153294046hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155755
SamplesHG00731
Known GenesFBXO5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567871
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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