A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928701



Internal ID22703945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68604139..68609593hg38UCSC Ensembl
chr16:68638042..68643496hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg385455
hg195455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv845n209
Supporting Variantsnssv17381125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928701
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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