A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939051



Internal ID22714440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86065641..86065751hg38UCSC Ensembl
chr16:86099247..86099357hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939051
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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