A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216133



Internal ID20783173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169187782..169213775hg38UCSC Ensembl
chr6:169587877..169613870hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3825994
hg1925994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216133
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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