A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188331



Internal ID20755371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10001..52800hg38UCSC Ensembl
chr16:60001..102800hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3842800
hg1942800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496145
Supporting Variants
Samples
Known GenesDDX11L10, MIR6859-1, MIR6859-2, POLR3K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188331
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00045


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