A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876347



Internal ID22651307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86605532..86628076hg38UCSC Ensembl
chr16:86639138..86661682hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3822545
hg1922545
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876347
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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