A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855160



Internal ID22630095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54895385..54897784hg38UCSC Ensembl
chr8:55807945..55810344hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855160
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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