A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194087



Internal ID20761127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98002737..98019812hg38UCSC Ensembl
chr12:98396515..98413590hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3817076
hg1917076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194087
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00715


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