A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857878



Internal ID22632813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20666961..20668060hg38UCSC Ensembl
chr8:20524472..20525571hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857878
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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