A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828093



Internal ID22603028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14534560..14535759hg38UCSC Ensembl
chr1:14861056..14862255hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460092, nssv17451703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828093
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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