A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406522



Internal ID21064075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21677627..21679454hg38UCSC Ensembl
chr6:21677858..21679685hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381828
hg191828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230872
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406522
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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