A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189905



Internal ID20756945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23059285..23106980hg38UCSC Ensembl
chr16:23070606..23118301hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3847696
hg1947696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495753
Supporting Variants
Samples
Known GenesUSP31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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