A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841813



Internal ID22616748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152204993..152220532hg38UCSC Ensembl
chr5:151584554..151600093hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3815540
hg1915540
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841813
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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