A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858476



Internal ID22633411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11389651..11416581hg38UCSC Ensembl
chr8:11247160..11274090hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3826931
hg1926931
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505013
Samples
Known GenesC8orf12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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