A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840353



Internal ID22615288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111519167..111531777hg38UCSC Ensembl
chr5:110854865..110867475hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3812611
hg1912611
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493066
Samples
Known GenesSTARD4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840353
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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