A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219472



Internal ID20786512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42014132..42024170hg38UCSC Ensembl
chr6:41981870..41991908hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3810039
hg1910039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413007
Supporting Variants
Samples
Known GenesCCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219472
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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