A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568882



Internal ID21517233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21851685..21852053hg38UCSC Ensembl
chr6:21851916..21852284hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151989
SamplesHG02011
Known GenesCASC15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568882
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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