A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858923



Internal ID22633858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42520471..42522570hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858923
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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