A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864643



Internal ID22639578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25657845..25665746hg38UCSC Ensembl
chr8:25515361..25523262hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg387902
hg197902
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508723
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864643
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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