A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851664



Internal ID22626599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22964821..22966620hg38UCSC Ensembl
chr8:22822334..22824133hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851664
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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