A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860965



Internal ID22635900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21836566..21840478hg38UCSC Ensembl
chr8:21694078..21697990hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383913
hg193913
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860965
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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