A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841976



Internal ID22616911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1846226..1851946hg38UCSC Ensembl
chr5:1846340..1852060hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg385721
hg195721
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841976
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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