A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841550



Internal ID22616485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16295085..16296187hg38UCSC Ensembl
chr5:16295194..16296296hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497026, nssv17497025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841550
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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