A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568766



Internal ID21517116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22659285..22659338hg38UCSC Ensembl
chr1:22985778..22985831hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062852
SamplesHG00513
Known GenesC1QB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568766
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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