A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568392



Internal ID21516739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158473770..158473836hg38UCSC Ensembl
chr1:158443560..158443626hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061222
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568392
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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