A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867721



Internal ID22642657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25507753..25511645hg38UCSC Ensembl
chr16:25519074..25522966hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383893
hg193893
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867721
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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