A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216941



Internal ID20783981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145366741..145383403hg38UCSC Ensembl
chr6:145687877..145704539hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3816663
hg1916663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216941
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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