A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861027



Internal ID22635962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42717099..42732310hg38UCSC Ensembl
chr8:42572242..42587453hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3815212
hg1915212
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506657
Samples
Known GenesCHRNB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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