A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404428



Internal ID21061981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27213145..27214812hg38UCSC Ensembl
chr6:27180924..27182591hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381668
hg191668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404428
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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