A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851171



Internal ID22626106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8992744..8995043hg38UCSC Ensembl
chr8:8850254..8852553hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851171
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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