A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216119



Internal ID20783159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168694236..168927295hg38UCSC Ensembl
chr6:169094677..169327390hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38233060
hg19232714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216119
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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