A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863850



Internal ID22638785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11866804..11867940hg38UCSC Ensembl
chr8:11724313..11725449hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505671, nssv17505672
Samples
Known GenesCTSB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863850
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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