A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179738



Internal ID20746778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20509301..20564500hg38UCSC Ensembl
chr16:20520623..20575822hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3855200
hg1955200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514834
Supporting Variants
Samples
Known GenesACSM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179738
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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