A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452776



Internal ID21110329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67841187..67850858hg38UCSC Ensembl
chr10:69600945..69610616hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg389672
hg199672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180911
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452776
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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