A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509867



Internal ID20883180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10001..117100hg38UCSC Ensembl
chr16:60001..167099hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38107100
hg19107099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177526
Samples
Known GenesDDX11L10, MIR6859-1, MIR6859-2, MPG, NPRL3, POLR3K, RHBDF1, SNRNP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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