A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568653



Internal ID21517002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46016093..46016142hg38UCSC Ensembl
chr6:45983830..45983879hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157855
SamplesNA19238
Known GenesCLIC5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568653
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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