A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841920



Internal ID22616855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177504786..177509400hg38UCSC Ensembl
chr5:176931787..176936401hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384615
hg194615
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494971
Samples
Known GenesDOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841920
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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