A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840887



Internal ID22615822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108997519..109012702hg38UCSC Ensembl
chr5:108333220..108348403hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3815184
hg1915184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499377
Samples
Known GenesFER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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