A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854901



Internal ID22629836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79376689..79377788hg38UCSC Ensembl
chr8:80288924..80290023hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509972, nssv17509973
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854901
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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