A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843659



Internal ID22618594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114060878..114062977hg38UCSC Ensembl
chr6:114382042..114384141hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500946
Samples
Known GenesHS3ST5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843659
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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