A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928536



Internal ID22703777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27369539..27370237hg38UCSC Ensembl
chr16:27380860..27381558hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928536
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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