A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18004859



Internal ID20571900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89535581..89541620hg38UCSC Ensembl
chr12:89929358..89935397hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg386040
hg196040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459692
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18004859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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