A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496145



Internal ID20869343
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 StatusM
Merged Variants
Supporting Variantsnssv18188331
Samples
Known GenesDDX11L10, MIR6859-1, MIR6859-2, POLR3K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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