A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930983



Internal ID21351052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50414371..50414371hg38UCSC Ensembl
chr16:50448282..50448282hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184729
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930983
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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