A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852422



Internal ID22627357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113443196..113447321hg38UCSC Ensembl
chr8:114455425..114459550hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg384126
hg194126
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852422
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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