A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846386



Internal ID22621321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98147667..98150177hg38UCSC Ensembl
chr6:98595543..98598053hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg382511
hg192511
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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