A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177526



Internal ID20744566
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 StatusS
Merged Variantsnsv6509867
Supporting Variants
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)nssv18177526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00026


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