A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856789



Internal ID22631724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85016597..85019584hg38UCSC Ensembl
chr8:85928832..85931819hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg382988
hg192988
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856789
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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