A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850998



Internal ID22625933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121054984..121057200hg38UCSC Ensembl
chr8:122067224..122069440hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg382217
hg192217
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850998
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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