A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844210



Internal ID22619145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108757512..108762036hg38UCSC Ensembl
chr6:109078715..109083239hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384525
hg194525
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500901
Samples
Known GenesLINC00222
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844210
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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