A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841491



Internal ID22616426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151631022..151632666hg38UCSC Ensembl
chr5:151010583..151012227hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381645
hg191645
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496299, nssv17496298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841491
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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