A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410072



Internal ID21067625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89052135..89055389hg38UCSC Ensembl
chr6:89761854..89765108hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383255
hg193255
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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