A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844826



Internal ID22619761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21361517..21366819hg38UCSC Ensembl
chr6:21361748..21367050hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385303
hg195303
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844826
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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