A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642056



Internal ID21590361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21980565..21980565hg38UCSC Ensembl
chr6:21980794..21980794hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152346
SamplesHG02818
Known GenesCASC15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642056
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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