A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841483



Internal ID22616418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148860045..148862419hg38UCSC Ensembl
chr5:148239608..148241982hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382375
hg192375
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841483
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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