A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844289



Internal ID22619224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13416039..13448900hg38UCSC Ensembl
chr6:13416271..13449132hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3832862
hg1932862
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501603
Samples
Known GenesGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844289
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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