A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413007



Internal ID21070560
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 StatusM
Merged Variants
Supporting Variantsnssv18219472
Samples
Known GenesCCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413007
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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