A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876453



Internal ID22651414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85975356..85980540hg38UCSC Ensembl
chr16:86008962..86014146hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385185
hg195185
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876453
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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