A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943791



Internal ID22719245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9802422..9802526hg38UCSC Ensembl
chr16:9896279..9896383hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387924
Samples
Known GenesGRIN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943791
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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