A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179312



Internal ID20746352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105673000..105857810hg38UCSC Ensembl
chr12:106066778..106251588hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38184811
hg19184811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455644
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179312
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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