A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396667



Internal ID21054220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14865471..14882076hg38UCSC Ensembl
chr6:14865702..14882307hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3816606
hg1916606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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